Title of Invention	"AN IMPROVED PROCESS FOR THE PREPARATION OF ARALKYLATED AROMATIC COMPUONDS USING HETEROGENEOUS CATALYST"
Abstract	The present invention relates to an improved process for the preparation of aralkylated aromatic compounds by catalytic alkylation of aromatic compounds with aromatic alkylating agent using a solid catalyst comprising gallium. The process for this invention can be used for the preparation of alkylated aromatic compounds, which are fine chemicals and/or used in the preparation of fine chemicals. Further, the process utilizes a active solid catalyst that can be reused repeatedly for the catalytic reaction.

Title of Invention

"AN IMPROVED PROCESS FOR THE PREPARATION OF ARALKYLATED AROMATIC COMPUONDS USING HETEROGENEOUS CATALYST"

Abstract

The present invention relates to an improved process for the preparation of aralkylated aromatic compounds by catalytic alkylation of aromatic compounds with aromatic alkylating agent using a solid catalyst comprising gallium. The process for this invention can be used for the preparation of alkylated aromatic compounds, which are fine chemicals and/or used in the preparation of fine chemicals. Further, the process utilizes a active solid catalyst that can be reused repeatedly for the catalytic reaction.

Full Text	This invention relates to an improved process for the preparation of aralkylated aromatic compound using heterogeneous catalyst, by catalytic alkylation of aromatic compound with aromatic alkylating agent using a solid catalyst. This invention particularly relates to the preparation of aralkylated aromatic compound by catalytic alkylation of aromatic compound with aromatic alkylating agent using a solid catalyst comprising of gallium. The process for this invention could be used for the preparation of alkylated aromatic compounds, which re fine chemicals and/or used in the preparation of fine chemicals. Aralkylated aromatic compounds are useful fine chemicals, these are also used as intermediates in a number of organic synthesis. Both the homogenous and heterogeneous catalyzed liquid phase processes for the preparation of aralkylated aromatic compounds are known in the prior art. Homogeneous Acid Catalyzed Processes According to a US patent US 3,678,122 [1972], diphenylmethane was prepared by treating a mixture of benzene and benzyl chloride with CuCl2. A US patent, US 3,679,760 [1972] disclosed the preparation of diaryl alkanes by refluxing benzyl chloride C6H4R1R2 (where R1= H and R2 = H, CH3 or OH) and CuCl2. A French patent, Fr. Demande 2,144,578 [1973], disclosed that substituted phenols p-RC6H4OH [where R=halogen or C1 to C4 alkyl] are benzylated by benzyl halides in the presence of ZnCl2. A USSR patent, USSR 394,353 [1973] disclosed preparation of 2,6 and 2,4 - (CH3O)2 C6H3CH2C6H5 by treating m-(CH3O)2 C6H4 with benzyl chloride in the presence of SnSO4 catalyst at 145 to 150 degree C, or SnCl2 catalyst at 165 to 170 degree C. A Japanese patent, Japan Kokai 7399,154 [1973], disclosed preparation of dibenzyl benzene derivatives by benzylation of benzene or substituted benzenes using Friedel-Crafts catalyst e.g., A1C13, FeCl3 and 98% H2S04. According to this patent, 200 g a-methyl benzyl chloride was added to a refluxing mixture of 500 g benzene and 5 g A1C13 and the whole mixture refluxed for 5h to give 120 g α-methyl bezylbenzene. According to a German patent, Ger. Offen 2,456,747 (1976), o-benzyltoluenes were prepared in -90% yields by the reaction of a o-chloromethyltoluene with a benzene derivative in > 1:7 ratio in the presence of H2SO4 and/or H3PO4 and optionally 4-CH3C6H4S03H, ZnCl2, BF3) etc.. Thus 135 parts 85% H3P04, 270 parts 85% H2S04, 10 parts 4-CH3C6H4S03H, 70 parts 2CH3C6H4CH2C1 and 390 parts of C6H6 were heated at 75-80° C for 4h to give 89% 2-CH3C6H4CH2C6H5. An US Patent U.S. 4,049,733 (1977), disclosed preparation of diphenylmethane by benzylation of benzene with benzylether using phosphoric acid and optionally H2S04 or a Friedel-Crafts type metal halide. European patent, Eup.Pat.Appl.EP 37,628 (1981), disclosed preparation of diphenylmethane by benzylation of benzene with chloromethylbenzenes in the presence of H2S04 and a cationic surfactant or a non-ionic surfactant which is susceptible to protonation under strong acidic conditions. A German patent, Ger.Offen DE 3,922,518 (1991), disclosed a process for the manufacture of a-methylbenzylphenol derivatives, which comprises the treatment of dwj-alkyl substituted phenols with styrene in the presence of phosphorus chloride catalyst. More recently, an European Patent, Eur.Pat.Appl.EP 538,704 (1993), disclosed a process for the preparation of p- substituted o-benzylphenols by treating phenols, p-RC6H4OH (R = halo, alkyl, OH, alkoxy, alkylmercapto, aryl, aryloxy or arylmercapto), with ArCH2X (Ar = corresponding aryl nucleus; X = halo, arylcarboxy, phenylsulfatoxy, hydroxy, alkoxy etc.) in a continuously functioning distillation apparatus in the presence of dissolved acid catalyst. The main disadvantages of the homogeneous acid catalyzed processes are as follows: 1) The separation and recovery of the dissolved acid catalysts from the liquid reaction mixture is difficult. 2) The disposal of the used acid catalysts creates environmental pollution. 3) The homogeneous acid catalysts also pose several other problems such as high toxicity, corrosion, spent acid disposal and use of more than the stoichiometric amount. Heterogeneous acid catalyzed processes. A German patent, Ger.Offen 2,547,030(1977), disclosed the preparation of o-benzyltoluenes by the reaction of o-methylbenzyl halides with substituted benzenes in the presence of Al-silicate. The 2-CH3C6H4CH2Cl was stirred with toluene and Al-silicate (25%Al203) at 110°C to give 81% 2-methylbenzyltoluene. According to a Japanese patent, Jpn. Kokai Tokkyo Koho JP 59,186,937 (1984), o-benzylphenol was prepared by the liquid phase reaction of benzyl alcohol with phenol in the presence of γ-Al2O3. For example 7.5 g γ-Al203 was added to a mixture of 32.5 g benzyl alcohol and 47 g phenol at 190°C under stirring to give a product containing 49.9% o-benzylphenol. A German Patent, Ger. Offen DE 3,700,917(1988), disclosed the preparation of p-substituted o-benzylphenols by benzylation of p-substituted phenols with benzylalcohol in the presence of Na-Y type zeolite. A mixture of 0.5 mole 4-ClC6H4OH, 0.1 mole C6H5CH2OH and 0.6 g of Na-Y type zeolite was heated at 200°C for 3 hrs to give 25.4 % 2-benzyl-4-chlorophenol. , A German patent, Ger. Offen DE 3,836,780 (1990), disclosed the process for the preparation of benzylbenzenes from benzenes and benzyl alcohols in the presence of activated bleaching earth and a diluent at 90-140°C. According to Japanese patent, Jpn Kokai Tokkyo Koho JP 03,170,442 (1991), benzylbiphenyls are manufactured by benzylating biphenyl and diphenylmethane with > 1 compound from benzyl halides, benzyl alcohol, benzyl ether in the presence of a zeolite or silica-alumina catalyst. An European patent, Eur.Pat. appl. EP 428,081 (1991), disclosed a process of benzylation of alkylbenzenes with benzyl chloride in the presence of H-Y or H-L zeolite catalyst. According to a German patent, Ger. Offen DE 4,038,933 (1992). disclosed a process for benzylation of aromatics using technical carbon catalysts. Aralkylation of aromatic compounds by aralkylating agent involves electrophilic substitution of H from the aromatic nucleus. It is well known in the prior art that the electrophilic substitution is favoured by the presence of electron donating groups, such as OH, alkyl, alkoxy, phenoxy, amine, alkyl amine, SH etc., in the aromatic compound to be aralkylated. Whereas the electrophilic substitution is inhibited by the presence of electron withdrawing groups such as halo, nitro, cyano, carboxy, aldehyde, etc., in the aromatic compound to be aralkylated. [ref. G.A.Olah, in Friedel-Crafts and related reactions, Wiley-Interscience Publ., New york, 1963]. Although some limitations of the homogeneous acid catalyzed processes are overcome by the prior art heterogeneous catalyzed processes described above, the aralkylating activity of the solid catalysts used in the prior art processes are low, particularly for aralkylating aromatic compounds containing electron withdrawing groups. Hence there is a great practical need for finding more efficient solid catalyst for the aralkylating of aromatic compounds. There is also a need for finding highly efficient solid catalyst also for the aralkylating of aromatic compounds containing electron withdrawing groups such as halo, nitro, cyano, carboxy, aldehyde, etc.. This invention is, therefore, made with the following objects so that most of the drawbacks or limitations of the prior art homogeneous and heterogeneous catalyzed processes for the preparation of aralkylated aromatic compounds could be overcome. 1. Accordingly, the main object of this invention is to provide a liquid phase process for the preparation of aralkylated aromatic compound by aralkylating aromatic compound with aralkylating agent, using a highly active solid catalyst comprising of gallium, which has high activity not only when the aromatic ring activating groups (i.e. electron donating groups) are present in the aromatic ring to be aralkylated but also when aromatic ring deactivating groups (i.e. electron withdrawing groups) are present in the aromatic ring to be aralkylated, so that the reaction temperature is low and/or time for completing the reaction is short. 2. Another important object of this invention is to provide a liquid phase process for the preparation of aralkylated aromatic compound by aralkylating aromatic compound with aralkylating agent, using highly active solid catalyst comprising of gallium, which can be reused repeatedly for the catalytic reaction. This invention provides a process for the preparation of aralkylated aromatic compound, represented by a general chemical formula: R1R2R3R4QCnH2nC6H3R5R6, having structural formula (1) of the drawing accompanying the specification by the aralkylation of aromatic compound, represented by a general chemical formula: R1R2R3R4M, having structural formula (2) of the drawing accompanying the specification with aralkylating agent, represented by a general chemical formula : R5R6 C6H3H2nX , having structural formula (3) of the drawing accompanying the specification wherein Q is C6H1 or C10H3 orC14H5; M is C6H2 or C10H4 or C14H6; each of RI, R2) R3 and R4 groups is H or CnH2n-n or CpH2p-1or C6H5 or CnH2nC6H5 or OH or OCnH2n+1 or OC6H5 or halogen or CnH2n+1xYv or N02 or NH2 or NHC,,H2n+1 or N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1 or COCnH2n+1 or S03H or SO3CnH2n-n or SH or alkyl mercapto group or aryl mercapto group; each of R5 and R6 group is H or CH3 or C2H5 or OH or OCH3 or OC2H5 or N02 or halogen or NH2; X is halogen or OH or SO3H or COOH or OCnH2nC6H5 or OCnH2n+1 or aryl carboxy group or alkyl carboxy group , x is an integer between 1 and 2n+l and n & p are integers greater than or equal to 1 and 2, respectively, and C,H,N,O and S are chemical elements, using a solid catalyst comprising gallium, which comprises: i) pretreating said solid catalyst at a temperature between about 100°C and about 800°C in a flow of moisture-free air or inert gas at a gas hourly space velocity in the range 1000-20000 cm3g-1'h-1'or under vacuum, for a period between about 0.1 hand about lOh. ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating agent having a mole ratio of said aromatic compound to the said aromatic aralkylating agent between about 0.5 and about 50, in the absence or presence of a suitable solvent selected from nitrobenzene, nitromethane and liquid paraffinic hydrocarbons, with a mole ratio of said solvent to said aralkylating agent between about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid catalyst to said aromatic aralkylating agent between about 0.02 and about 2.0 in a stirred batch reactor fitted with a reflux condenser, under vigorous stirring, while bubbling continuously a moisture-free inert gas, such as helium, nitrogen or argon, through the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1 cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the reaction to occur at a temperature between about 25°C and about 300°C at a pressure between about 1 atm and about 10 atm for a reaction period between about 0.01 h and about 50 h, and iii) cooling the reaction mixture to a temperature about 25°C, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art. The main finding of this invention is that, the said catalyst shows high activity in the aralkylation of aromatic compounds not only when the electron donating group, which is aromatic ring activating group, is present in the aromatic ring to be aralkylated but also when the electron withdrawing group, which is aromatic ring deactivating group, is present in the aromatic ring to be aralkylated, so that the reaction temperature is low and/or the time required for completing the reaction is short. Other important finding of this invention is that solid catalyst can be reused repeatedly in the aralkylation of said aromatic compounds. Yet another important finding of this invention is that the mechanism of the aralkylation of aromatic compounds over said solid catalyst is different from that of acid catalyzed Friedel-Crafts aralkylation reaction. Accordingly, the present invention provides an improved process for the preparation of aralkylated aromatic compound, represented by the formula R1R2R3R4QCnH2nC6H3R5R6, having structural formula (1) of the drawing accompanying the specification by the aralkylation of aromatic compound, represented by a the chemical formula R1R2R3R4M, having structural formula (2) of the drawing accompanying the specification with aralkylating agent, represented by a formula R5R6C6H3H2--nX, having structural formula (3) of the drawing accompanying the specification, wherein Q is C6H1 or C10H3 or C14H5; each of R1, R2, R3 and R4 groups is H or CnH2n+1 or CpH2p+1or C6Hs or CnH2n C6Hs or OH or PCnH2n+1 or OC6H5 or halogen or CnH2n+1-xYx or NO2 or NH2 or NHCnH2n+1or N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1 or COCnH2n+1 or SO3H or SO3CnH2n+1or SH or alkyl mercapto group or aryl mercapto group; each of R5 and R6 group of H or CH3 or C2H5 or OH or OCH3 or OC2H5 or NO2 or halogen or NH2 ; X is halogen or OH or SO3H or COOH or OCnH2n+1 or aryl carboxy group or alkyl carboxy group, x is an integer between 1 and 2n+l and n & p are integers greater than or equal to 1 and 2, respectively, and C, H, N, O and S are chemical elements, using a solid catalyst comprising gallium, which comprises: i) pretreating said solid catalyst at a temperature between 100°C and 800°C in a flow of moisture-free air or inert gas at a gas hourly space velocity in the range 1000 - 2000 cm3 g-1h-1 or under vacuum, for a period between about 0.1 h and about 10 h; ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating agent having a mole ratio of said aromatic compound to the said aromatic aralkylating agent between 0.5 and 50, in the absence of presence of a suitable solvent selected from nitrobenzene, nitro methane and liquid paraffmic hydrocarbons, with a mole ratio of said solvent to said alkylating agent between about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid catalyst to said aromatic alkylating agent between 0.02 and 2.0 in a stirred batch reactor fitted with a reflux condenser, under vigorous stirring, while bubbling continuously a moisture-free inert gas, such as helium, nitrogen or argon, through the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1 cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the reaction to occur at a temperature between 20°C and 300°C at a pressure between 1 atm and 100 atm for a reaction period between 0.01 h and 50 h, and iii) cooling the reaction mixture to room temperature, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art. In the process of the present invention, the preferred reaction temperature is between about 50°C and about 200°C; the preferred reaction pressure is between about 1 atm and about 5 atm; the preferred reaction period is between about 0.05 h and about 20 h; the preferred mole ratio of said aromatic compound to said aralkylating agent is between about 1 and about 20; the preferred weight ratio of said catalyst to said aralkylating agent is between about 0.05 and about 0.5. In the process of the present invention, a preferred said catalyst is selected from micro or mesoporous gallosilicates and galloaluminosilicates, having structure similar to that of zeolites known in the prior art; Ga+3- exchanged micro and mesoporous zeolites and cationic clays; micro or mesoporous gallophosphatcs or galloaluminophosphates; Ga2O3 and /or Ga-halide impregnated or deposited on micro and mesoporous zeolites, crystalline micro and mesoporous alumino- and metallo- phosphates, cationic and anionic clays, microporous and mesoporous metal oxides or mixed metal oxides and macroporous catalyst supports; gallium oxide pillared clays; and gallium oxide. A more preferred said catalyst for the process of this invention is selected from H-gallo- and H-galloalumino-silicates of ZSM-5 and MCM-41 type zeolites; Ga2O3 or Ga2O3 deposited on H-ZSM-5 zeolite, MCM-41 zeolite macroporous catalyst supports comprising of silica, alumina, silicon carbide or ZrO2 and HID2 or their mixture; and GaCl3 impregnated on Montmorillonite K10 clay or high silica MCM-41. The process of this invention can be carried out in a stirred batch reactor, fitted with a reflux condenser and arrangement for bubbling inert gas through the reaction mixture, known in the prior art for carrying out liquid phase reactions. In the process of this invention, the main products formed are said aralkylated aromatic compound and a by-product HX, wherein H = hydrogen and X = halogen or OH or SO3H or COOH or OCnH2nC6H5 or OCnH2n+1 or arylcarboxy group or alkylcarboxy group, depending upon said aralkylating agent used. In the process of this invention, said aromatic compound and said aralkylating agent are reactants and are converted partially or completely to said products. In the process of this invention, the role of said solvent, if used, is to dissolve solid reactant or reactants, to dilute reactants and/or to facilitate the reaction between said aromatic compound and said aralkylating agent. However, solvent may not be used in the process of this invention when both the reactants are liquid at said reaction conditions. Normally, said solvent is not converted in the process of this invention. In the process of this invention, the role of inert gas bubbling continuously through the reaction mixture is to remove continuously said by-product from the reaction mixture so that the reverse reaction is avoided or minimised and the time required for completing the reaction is shortened. In the process of this invention, the role of the reflux condenser fitted with the reactor is to condense reactants and solvents and to return them back to the reaction mixture and allow the inert gas, which is continuously bubbling through the reaction mixture, along with said by-product to escape from the reaction mixture. In the process of this invention, the reaction pressure above atmospheric pressure may be used to allow the reaction to be carried out at temperature higher than the normal boiling point of the reactants and/or solvent, by increasing the boiling point of said reactants and/or solvent with increasing the reaction pressure. Said catalyst, used in the process of this invention, is heterogeneous with respect to the reaction mixture and can be removed from the reaction mixture simply by filtration and the removed catalyst, after washing with solvent or said liquid aromatic compound which is to be aralkylated, can be reused in the said process. Said pretreatment to said catalyst in step-i of the process of present invention is necessary for removing moisture adsorbed on the catalyst so that the catalyst shows its full efficiency for catalysing the reaction between said aromatic compound and said aralkylating agent. The role of gallium compound present in said catalyst is to activate both the reactants, said aromatic compound and said aralkylating agent. The R5R6C6H3CnH2n----X bond of said aralkylating agent is weakened by its interaction with said gallium compound, leading to the formation of a stable carbocation [R5R6C6H3CnH2nr (I) and X~ . In the presence of said carbocation (I), said aromatic compound is activated on gallium compound by weakening its bond between aromatic nucleus and H, leading to the formation of a penta-coordinated carbocation by the combination of said activated aromatic compound and said carbocation (I). The said penta-coordinated carbocation is then decomposed to said aralkylated aromatic compound, the main product of the reaction, and a proton, which combines with X~ to give HX, the by-product of the reaction. Said catalyst used in the process of invention can be prepared by various methods, such as hydrothermal synthesis, impregnation, coating, cation exchange, coprecipitation and pillaring of clays, all known in the prior art. Zeolites are crystalline aluminosilicates containing well defined channels or pores of uniform diameter. A large number of microporous zeolites, such as X, Y, mordenite, L, beta, ZSM-5, ZSM-8, ZSM-11, etc., and mesoporous zeolites, such as M41S type material, e.g. MCM-41, are known in the prior-art. [ ref. Breck in Zeolite Molecular Sieves, Wiley-Interscience Publ., New York, 1974; Beck and Co-workers. J.Am.Chem.Soc., vol.114, page 10834,year 1992; Nature (London) vol.359, page 710, year 1992]. In general, micropores have diameter below 1 run; mesopores have diameter between about 1 nm and about 20 nm; and macropores have diameter above about 20 nm. Said catalyst containing only micropores may be used in the process of this invention when both the reactants have minimum molecular diameter or critical size less than 0.7 nm. Whereas said catalyst containing meso and/or macropores may be used in the process of this invention for both small and large molecular size reactants. By the process of this invention, benzene, nitrobenzene (which contains highly deactivating electron withdrawing group NCh) and anthracene can be benzylated with benzyl chloride to corresponding aralkylated aromatic compound with a benzyl chloride conversion of 95%, 95% and 95%, respectively, at 1 atm pressure, temperature 80°C, 135°C and 130°C, respectively and reaction period 0.16 h, 0.27 h and 0.31 h, respectively, using Ga2O3 (10 wt %) supported on commercial low surface area ( The present invention is described with respect to the following examples illustrating the process of this invention for the preparation of aralkylated aromatic compounds. These examples are provided for illustrative purposes only and are not to be construed as limitations on the process of this invention. Definition of terms used in the examples Conversion of reactant (%) = mole % of the reactant converted to all products. All the ratios of said aromatic compounds to said aralkylating agent and of said solvent to said aralkylatying agent are mole ratios. The said catalyst to the said aralkylating agent ratio is weight ratio. The flow rates of gases are measured at 0°C and 1 atm pressure. Gas hourly space velocity (GHSV) is volume of gas, measured at 0°C and 1 atm pressure, passed over unit mass of catalyst per hour. Ac and Aa represent aromatic compound to be aralkylated and aralkylating agent, respectively. The micropores, mesopores and macropores have pore diameter of below 1.0 nm, between about 1.0 nm and about 20 nm, and above about 20 nm, respectively. EXAMPLE-1 This example illustrates the process of this invention for the benzylation of benzene, nitrobenzene, m-xylene, p-xylene, durene (1,2,4,5 tetramethylbenzene ), napthalene and anthracene by benzyl chloride or benzyl bromide to the corresponding benzylated aromatic compounds , using Ga2O3 supported on a commercial macroporous silica alumina (SA 5205) catalyst carrier as a catalyst. The supported Ga2O3catalyst, Ga203 (10 wt. %)/SA 5205, was prepared by depositing the required amount of gallium nitrate from its aqueous solution on the commercial support SA 5205 (obtained from M/s. NORTON Co. U.S.A.), having main chemical composition : 11.8 % Si02 , 86.1 % A1203 ; surface area The catalytic benzylation reaction over the Ga2O3 / SA 5205 was carried out by i) pretreating the catalyst in a quartz tubular reactor under a flow of moisture-free helium at a gas hourly space velocity of 18,000 cm 3 g-1' h-1 at 400 °C for 1 h ,and then ii) contacting said pretreated catalyst with 15 cm3 liquid reaction mixture containing aromatic compound to be benzylated and the benzylating agent and optionally a solvent, in a stirred batch reactor (capacity : 50 cm3) fitted with a reflux condenser, mercury thermometer dipped in the reaction mixture and an inlet tube for passing gas through the reaction mixture, under vigorous stirring, while bubbling moisture-free N2 gas through the reaction mixture at the reaction conditions given in TABLES-1 and 2 and following the course of the reaction by measuring quantitatively the HC1 or HBr evolved during the reaction by absorbing it in aqueous NaOH solution by a simple acid-base titration using phenolphthalein indicator, and iii) cooling the reaction mixture to room temperature (25°C) and analysing the products and unconverted reactants present in the reaction mixture, after separating the solid catalyst from it by filtration, using chromatographic technique. The results are included in TABLES-1 and 2. TABLE-1 : Reaction conditions and results of the aralkylation of different aromatic compounds over Ga203(10 wt%)/SA 5205 catalyst. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent TABLE-2 : Reaction conditions and results of the aralkylation of different aromatic compounds over Ga2O3(10 wt%)/SA 5205 catalyst. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent EXAMPLE-2 This example illustrates the process of this invention for the benzylation of benzene and different substituted benzenes by benzyl chloride or benzyl alcohol, as an aralkylating agent, to corresponding benzylated aromatic compounds, using ZSM-5 type microporous H-galloalumino silicate, as a catalyst, in powder form. The ZSM-5 type H-galloalumino silicate, having Ga/Al = 3, Si/(Al+Ga) = 11.7, and degree of H+ exchange >98% and crystal size = 4-6µm, was prepared by the procedure known in the prior art [ref. Choudhary et al., Journal of Catalysis, vol. 158, page 23 and year 1996; Zeolites vol. 18, page 274 and year 1997 ]. The catalytic benzylation of benzene and substituted benzenes by benzyl chloride or benzyl alcohol over the H-galloalumino silicate catalyst was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLES-3 and 4. The results are included in TABLES-3 and 4. TABLE-3 : Reaction conditions and results of the aralkylation of different aromatic compounds over a solid catalyst, H-galloalumino silicate of ZSM-5 type. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent TABLE-4 : Reaction conditions and results of the aralkylation of different aromatic compounds over a solid catalyst, H-galloalumino silicate of ZSM-5 type. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent EXAMPLE 3 This example illustrates the process of this invention for the preparation of benzyl benzene and benzyl toluene by benzylation of benzene and toluene, respectively, with benzyl chloride in the absence of any solvent, over H-gallosilicate of ZSM-5 type , as a catalyst, in the form of powder. The H-gallosilicate (ZSM-5 type), having Si/Ga=33 and degree of H+ exchange >95%and crystal or particle size = 5-6 µm, was prepared by the procedure described earlier [ref. Choudhary et al., Journal of Catalysis, volume 158, page 34 and year 1996 ]. The catalytic benzylation of benzene and toluene by benzyl chloride over H-gallosilicate catalyst was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLE-5, except that the catalyst pre-treatment was carried out under vacuum (2 torr pressure ) at 600°Cfor 0.5 h. The results are included in TABLE-5. TABLE-5 : Reaction conditions and results of the aralkylation of benzene and toluene over H-gallo'silicate of ZSM-5 type, as a catalyst. (Table Removed) Ac = Aromatic compound, Aa - Aralkylating agent EXAMPLE-4 This example illustrates the process of this invention for the preparation of aralkylated benzene by the aralkylation of benzene with different aralkylating agents, using Ga203 (obtained from M/s Aldrich Chemicals, U.S.A.) and Ga2O3 supported on microporous H-ZSM-5 and silica gel, micro and mesoporous y-Al2O3 and mesoporous high silica MCM-41, as catalysts, in the absence of any solvent. The Ga2O3 (3.0 wt.%)/H-ZSM-5, Ga203 (10 wt.%)/SiO2 gel, Ga2O3 (10 wt.%)/ y-Al2O3 and Ga2O3 (10 wt.)/highsilica MCM-41 catalysts were prepared by depositing the required amount of gallium nitrate from its aqueous solution on H-ZSM-5 (Si/Al =35.0, degree of H+ exchange >99.0 % and crystal size 3-5 jam), silica gel (Fuji Davison, A-type, surface area 720 m2g-1), y-Al203 (surface area 155 m2g-1) and high silica MCM-41 [prepared by the procedure described in the ref. Choudhary et al., Proceeding of Indian Academy of Sciences, (Chemical Sciences) volume 109, page 229 and year 1997], respectively, in powder form, by incipient wetness technique, drying the impregnated mass at 120°C for 10 h and calcining at 500°C for 6 h. The catalytic aralkylation of benzene by different aralkylating agents over each of the above catalysts was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLE-6, except that in the present case the pretreatment of the catalyst was carried out in the flow of moisture-free N2 at 500°C at a gas hourly space velocity of 3000 cm3 .g-1.h11 for 2 h. The results are included in TABLE-6. The results in TABLE-6 show that the Ga2O3 and supported Ga2O3 catalysts except Ga203./ γ-Al203) show high activity in the benzylation of benzene. However, it may be noted that the support alone, i.e. H-ZSM-5 zeolite, silica gel, γ- alumina and high silica MCM-41 zeolite, showed no activity in the benzylation of benzene at the said reaction conditions. TABLE-6 : Reaction conditions and results of the aralkylation of benzene over Ga203 supported on different catalyst carriers, as a catalyst. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent EXAMPLE-5 This example illustrates the process of this invention for the benzylation of benzene and substituted benzenes by benzyl chloride to corresponding benzylated aromatic compounds, using GaCl3 impregnated Montmorillonite K10 clay catalyst in the absence of a solvent. The GaCl3 (10 wt.%)/MontmoriIlonite K10 clay catalyst was prepared by impregnating required amount of GaCl3 from its dry acetonitrile solution on Montmorillonite K10 clay (obtained from Aldrich Chemicals co. U.S.A.) in powder form, following the incipient wetness technique and drying the impregnated mass at 60°C under vacuum for 10 h. The catalytic benzylation of benzene and substituted benzenes by benzyl chloride over the above catalyst has been carried out by the procedure same as that described in EXAMPLE-1, at the reaction conditions given in TABLE-7, except that in the present case the pretreatment of the catalyst was carried out at 120 °C in the flow of moisture-free helium gas at a gas hourly space velocity of 6000 cmjg -1 h-1 for 5 h. The results are included in TABLE-7. TABLE-7 : Reaction conditions and results of the aralkylation of different aromatic compounds over GaCl3/Montmorillonite K1Q, as a catalyst. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent EXAMPLE-6 This example illustrates the process of this invention for the benzylation of toluene by benzyl chloride using Ga2O3/SA 5205 catalyst prepared in EXAMPLE-1, and reused of this catalyst for the subsequent reactions carried out in a number of batches. The benzylation reactions was carried out using the Ga2O3/SA 5205 catalyst, prepared in EXAMPLE-1, and by the procedure same as that described in EXAMPLE-1, at the reaction conditions given in TABLE-8, except that in the present case the catalyst used in the second and onward batches was not given said pretreatment, Instead the catalyst obtained by filtration from the reaction mixture of first batch was used as it is, after washing it with toluene, for the second batch reaction, and so on. The results are given in TABLE-8. The results show that the catalyst can be reused repeatedly for the process. TABLE-8 : Reaction conditions and results of the aralkylation of toluene by benzyl chloride over Ga2O3(10 wt%)/SA 5205 catalyst, fresh and reused in the subsequent batches. (Table Removed) Ac = Aromatic compound, Aa = Aralkylating agent The main advantages of the process of this invention over the prior art processes for the preparation of aralkylated aromatic compounds are as follows: 1) The process of this invention has a number of advantages over the earlier homogeneous catalysed processes for the preparation of aralkylated aromatic compounds, as follows: In the process of this invention i) the catalyst used is heterogeneous solid catalyst and hence it can be separated T from the reaction products simply by filtration , ii) the separated catalysts can be reused in the process for a number of times, and iii) also the catalyst is non corrosive, therefore most of the serious problems associated with homogeneous catalyst used in the earlier homogeneous catalysed processes for the preparation of aralkylated aromatic compounds are overcome m the process of this invention. 2) The process of this invention has also number of advantages over the prior art processes based on the use of solid catalyst for the preparation of aralkylated aromatic compounds, as follows: i) The activity of the said catalyst used in the process of present invention is higher. ii) The process of the present invention can be used for aralkyating both small and large size aromatic compounds with both small and large size aralkylating agents to produce the corresponding aralkylated compounds. iii) In the process of this invention, since moisture-free inert gas is bubbled through the reaction mixture continuously, said by-product formed in the reaction is removed continuously and thereby the reverse aralkylation reaction is avoided or minimised, thus requiring shorter time for completing the reaction, iv) In the process of this invention, it is possible to carry out the aralkylation reaction at a temperature higher than the normal boiling point of either of the reactants and the solvent, and thereby the reaction period for completing the reaction is shortened and/or the inhibition of the reaction due to strong adsorption of the reactants, products or solvent on the catalyst is avoided or minimised, v) By the process of this invention, the aralkylation of said aromatic compound is possible at mild reaction conditions even though when the aromatic compound does not contain any aromatic nucleus activating group or electron donating group, for example when aromatic compound is benzene, or when said aromatic compound contains electron withdrawing group, for example halide or nitro group, which has highly deactivating effect on the aromatic nucleus for the aralkylation reaction. We Claim: 1. An improved process for the preparation of aralkylated aromatic compound, represented by a general chemical formula: RiR2R3R4QCnH2nC6H3R5R6, having structural formula (1) of the drawing accompanying the specification by the aralkylation of aromatic compound, represented by a general chemical formula R1R2R3R4M, having structural formula (2) of the drawing accompanying the specification with aralkylating agent, represented by a general chemical formula : R5R6C6H3H2nX, having structural formula (3) of the drawing accompanying the specification wherein Q is C6H1 or C10H3 or C14H6; each of R1, R2, R3 and R4 groups is H or CnH2n+1 or CpH2p-1 or CeHs or CnH2n C6H5 or OH or PCnH2n+, or OC6H5 or halogen or CnH2n+1xYx or NO2 or NH2 or NHCnH2n+1or N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1 or COCnH2n+1 or SO3H or SO3CnH2n+1 or SH or alkyl mercapto group or aryl mercapto group; each of R5 and R6 group of H or CH3or C2H5 or OH or OCH3 or OC2H5or NO2 or halogen or NH2; X is halogen or OH or SO3H or COOH or OCnH2n+1 or aryl carboxy group or alkyl carboxy group, x is an integer between 1 and 2n+l and N & P are integers greater than or equal to 1 and 2, respectively, and C, H, N, O and S are chemical elements, using a solid catalyst comprising gallium, which comprises: i) pretreating said solid catalyst at a temperature between 100°C and 800°C in a flow of moisture-free air or inert gas at a gas hourly space velocity in the range 1000 - 2000 cm3 g-1h-1or under vacuum, for a period between about 0.1 h and about 10 h ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating agent having a mole ratio of said aromatic compound to the said aromatic aralkylating agent between 0.5 and 50, in the absence of presence of a suitable solvent selected from nitrobenzene, nitro methane and liquid paraffmic hydrocarbons, with a mole ratio of said solvent to said alkylating agent between about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid catalyst to said aromatic alkylating agent between 0.02 and 2.0 in a stirred batch reactor fitted with a reflux condenser, under vigorous stirring, while bubbling continuously a moisture-free inert gas, such as helium, nitrogen or argon, through the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1 cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the reaction to occur at a temperature between 20°C and 300°C at a pressure between 1 atm and 100 atm for a reaction period between 0.01 h and 50 h, and iii) cooling the reaction mixture to room temperature, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art. 2. An improved process as claimed in claim 1, wherein the reaction temperature is between 50°C and 200°C. 3. An improved process as claimed in claim 1, wherein the reaction pressure is between 1.0 atm to 5.0 atm. 4. An improved process as claimed in claim 1, wherein the reaction period ranges between 0.05 h and 20h. 5. An improved process as claimed in claim 1, wherein the mole ratio of said aromatic compound to said aralkylating agent is between 1 and 20. 6. An improved process as claimed in claim 1, wherein a weight ratio of said catalyst to said aralkylating agent is between 0.05 to 0.5. 7. An improved process as claimed in claim 1, wherein said catalyst is selected from micro or mesoporous Gallo silicates and galloaluminosilcates, having structure similar to that of zeolites; Ga+3 - exchanged micro and mesoporous zeolites and cationic clays; miro or mesoporous gallophosphates or galloaluminophosphates; Ga2O3 and/or Ga-halide impregnated or deposited on micro and mesoporous zeolites, crystalline micro or mespoporous alumino-, silico-alumino and metallophosphates, cationic and anionic clays, micro porous and mespoporous metal oxides or mixed metal oxides and macroporous ctalyst supports; and gallium oxide pillared clays; and gallium oxide. 8. An improved process as claimed in claims 1 and 7, wherein said catalyst is selected from -gallo-and H-galloalumino-silicated of ZSM-5 zeolite, MCM-41 zeolite and macroporous catalyst supports comprising of silica, alumina, silicon carbide or ZrO2 and HfO2 or their mixture; and GaCl3 impregnated on Montmorillonite K10 clay or high silica MCM-41. 9. An improved process for the preparation of aralkylated aromatic compound using solid catalyst comprising of gallium, substantially as herein described with reference to the examples.

Full Text

This invention relates to an improved process for the preparation of aralkylated aromatic compound using heterogeneous catalyst, by catalytic alkylation of aromatic compound with aromatic alkylating agent using a solid catalyst. This invention particularly relates to the preparation of aralkylated aromatic compound by catalytic alkylation of aromatic compound with aromatic alkylating agent using a solid catalyst comprising of gallium.
The process for this invention could be used for the preparation of alkylated aromatic compounds, which re fine chemicals and/or used in the preparation of fine chemicals.
Aralkylated aromatic compounds are useful fine chemicals, these are also used as intermediates in a number of organic synthesis. Both the homogenous and heterogeneous catalyzed liquid phase processes for the preparation of aralkylated aromatic compounds are known in the prior art.
Homogeneous Acid Catalyzed Processes
According to a US patent US 3,678,122 [1972], diphenylmethane was prepared by treating a mixture of benzene and benzyl chloride with CuCl2. A US patent, US 3,679,760 [1972] disclosed the preparation of diaryl alkanes by refluxing benzyl chloride C6H4R1R2 (where R1= H and R2 = H, CH3 or OH) and CuCl2.
A French patent, Fr. Demande 2,144,578 [1973], disclosed that substituted phenols p-RC6H4OH [where R=halogen or C1 to C4 alkyl] are benzylated by benzyl halides in the presence of ZnCl2. A USSR patent, USSR 394,353 [1973] disclosed preparation of 2,6 and 2,4 - (CH3O)2 C6H3CH2C6H5 by treating m-(CH3O)2 C6H4 with benzyl chloride in the presence of SnSO4 catalyst at 145 to 150 degree C, or SnCl2 catalyst at 165 to 170 degree C. A Japanese patent, Japan Kokai 7399,154 [1973], disclosed preparation of dibenzyl benzene

derivatives by benzylation of benzene or substituted benzenes using Friedel-Crafts catalyst e.g., A1C13, FeCl3 and 98% H2S04. According to this patent, 200 g a-methyl benzyl chloride was added to a refluxing mixture of 500 g benzene and 5 g A1C13 and the whole mixture refluxed for 5h to give 120 g α-methyl bezylbenzene.
According to a German patent, Ger. Offen 2,456,747 (1976), o-benzyltoluenes were prepared in -90% yields by the reaction of a o-chloromethyltoluene with a benzene derivative in > 1:7 ratio in the presence of H2SO4 and/or H3PO4 and optionally 4-CH3C6H4S03H, ZnCl2, BF3) etc.. Thus 135 parts 85% H3P04, 270 parts 85% H2S04, 10 parts 4-CH3C6H4S03H, 70 parts 2CH3C6H4CH2C1 and 390 parts of C6H6 were heated at 75-80° C for 4h to give 89% 2-CH3C6H4CH2C6H5.
An US Patent U.S. 4,049,733 (1977), disclosed preparation of diphenylmethane by benzylation of benzene with benzylether using phosphoric acid and optionally H2S04 or a Friedel-Crafts type metal halide.
European patent, Eup.Pat.Appl.EP 37,628 (1981), disclosed preparation of diphenylmethane by benzylation of benzene with chloromethylbenzenes in the presence of H2S04 and a cationic surfactant or a non-ionic surfactant which is susceptible to protonation under strong acidic conditions.
A German patent, Ger.Offen DE 3,922,518 (1991), disclosed a process for the manufacture of a-methylbenzylphenol derivatives, which comprises the treatment of dwj-alkyl substituted phenols with styrene in the presence of phosphorus chloride catalyst. More recently, an European Patent, Eur.Pat.Appl.EP 538,704 (1993), disclosed a process for the preparation of p- substituted o-benzylphenols by treating phenols, p-RC6H4OH (R = halo, alkyl, OH, alkoxy, alkylmercapto, aryl, aryloxy or

arylmercapto), with ArCH2X (Ar = corresponding aryl nucleus; X = halo, arylcarboxy, phenylsulfatoxy, hydroxy, alkoxy etc.) in a continuously functioning distillation apparatus in the presence of dissolved acid catalyst.
The main disadvantages of the homogeneous acid catalyzed processes are as follows: 1) The separation and recovery of the dissolved acid catalysts from the liquid reaction
mixture is difficult.
2) The disposal of the used acid catalysts creates environmental pollution.
3) The homogeneous acid catalysts also pose several other problems such as high
toxicity, corrosion, spent acid disposal and use of more than the stoichiometric
amount.
Heterogeneous acid catalyzed processes.
A German patent, Ger.Offen 2,547,030(1977), disclosed the preparation of o-benzyltoluenes by the reaction of o-methylbenzyl halides with substituted benzenes in the presence of Al-silicate. The 2-CH3C6H4CH2Cl was stirred with toluene and Al-silicate (25%Al203) at 110°C to give 81% 2-methylbenzyltoluene. According to a Japanese patent, Jpn. Kokai Tokkyo Koho JP 59,186,937 (1984), o-benzylphenol was prepared by the liquid phase reaction of benzyl alcohol with phenol in the presence of γ-Al2O3. For example 7.5 g γ-Al203 was added to a mixture of 32.5 g benzyl alcohol and 47 g phenol at 190°C under stirring to give a product containing 49.9% o-benzylphenol. A German Patent, Ger. Offen DE 3,700,917(1988), disclosed the preparation of p-substituted o-benzylphenols by benzylation of p-substituted phenols with benzylalcohol in the presence of Na-Y type zeolite. A mixture of 0.5 mole 4-ClC6H4OH, 0.1 mole

C6H5CH2OH and 0.6 g of Na-Y type zeolite was heated at 200°C for 3 hrs to give 25.4 % 2-benzyl-4-chlorophenol. ,
A German patent, Ger. Offen DE 3,836,780 (1990), disclosed the process for the preparation of benzylbenzenes from benzenes and benzyl alcohols in the presence of activated bleaching earth and a diluent at 90-140°C. According to Japanese patent, Jpn Kokai Tokkyo Koho JP 03,170,442 (1991), benzylbiphenyls are manufactured by benzylating biphenyl and diphenylmethane with > 1 compound from benzyl halides, benzyl alcohol, benzyl ether in the presence of a zeolite or silica-alumina catalyst. An European patent, Eur.Pat. appl. EP 428,081 (1991), disclosed a process of benzylation of alkylbenzenes with benzyl chloride in the presence of H-Y or H-L zeolite catalyst. According to a German patent, Ger. Offen DE 4,038,933 (1992). disclosed a process for benzylation of aromatics using technical carbon catalysts.
Aralkylation of aromatic compounds by aralkylating agent involves electrophilic substitution of H from the aromatic nucleus. It is well known in the prior art that the electrophilic substitution is favoured by the presence of electron donating groups, such as OH, alkyl, alkoxy, phenoxy, amine, alkyl amine, SH etc., in the aromatic compound to be aralkylated. Whereas the electrophilic substitution is inhibited by the presence of electron withdrawing groups such as halo, nitro, cyano, carboxy, aldehyde, etc., in the aromatic compound to be aralkylated. [ref. G.A.Olah, in Friedel-Crafts and related reactions, Wiley-Interscience Publ., New york, 1963].
Although some limitations of the homogeneous acid catalyzed processes are overcome by the prior art heterogeneous catalyzed processes described above, the aralkylating activity of the solid catalysts used in the prior art processes are low,

particularly for aralkylating aromatic compounds containing electron withdrawing groups. Hence there is a great practical need for finding more efficient solid catalyst for the aralkylating of aromatic compounds. There is also a need for finding highly efficient solid catalyst also for the aralkylating of aromatic compounds containing electron withdrawing groups such as halo, nitro, cyano, carboxy, aldehyde, etc.. This invention is, therefore, made with the following objects so that most of the drawbacks or limitations of the prior art homogeneous and heterogeneous catalyzed processes for the preparation of aralkylated aromatic compounds could be overcome.
1. Accordingly, the main object of this invention is to provide a liquid phase process for the preparation of aralkylated aromatic compound by aralkylating aromatic compound with aralkylating agent, using a highly active solid catalyst comprising of gallium, which has high activity not only when the aromatic ring activating groups (i.e. electron donating groups) are present in the aromatic ring to be aralkylated but also when aromatic ring deactivating groups (i.e. electron withdrawing groups) are present in the aromatic ring to be aralkylated, so that the reaction temperature is low and/or time for completing the reaction is short. 2. Another important object of this invention is to provide a liquid phase process for the preparation of aralkylated aromatic compound by aralkylating aromatic compound with aralkylating agent, using highly active solid catalyst comprising of gallium, which can be reused repeatedly for the catalytic reaction.

This invention provides a process for the preparation of aralkylated aromatic compound, represented by a general chemical formula:
R1R2R3R4QCnH2nC6H3R5R6, having structural formula (1) of the drawing accompanying the specification by the aralkylation of aromatic compound, represented by a general chemical formula: R1R2R3R4M, having structural formula (2) of the drawing accompanying the specification with aralkylating agent, represented by a general chemical formula : R5R6 C6H3H2nX , having structural formula (3) of the drawing accompanying the specification
wherein Q is C6H1 or C10H3 orC14H5; M is C6H2 or C10H4 or C14H6; each of RI, R2) R3 and R4 groups is H or CnH2n-n or CpH2p-1or C6H5 or CnH2nC6H5 or OH or OCnH2n+1 or OC6H5 or halogen or CnH2n+1xYv or N02 or NH2 or NHC,,H2n+1 or N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1 or COCnH2n+1 or S03H or SO3CnH2n-n or SH or alkyl mercapto group or aryl mercapto group; each of R5 and R6 group is H or CH3 or C2H5 or OH or OCH3 or OC2H5 or N02 or halogen or NH2; X is halogen or OH or SO3H or COOH or OCnH2nC6H5 or OCnH2n+1 or aryl carboxy group or alkyl carboxy group , x is an integer between 1 and 2n+l and n & p are integers greater than or equal to 1 and 2, respectively, and C,H,N,O and S are chemical elements, using a solid catalyst comprising gallium, which comprises:
i) pretreating said solid catalyst at a temperature between about 100°C and about 800°C in a flow of moisture-free air or inert gas at a gas hourly space velocity in the range 1000-20000 cm3g-1'h-1'or under vacuum, for a period between about 0.1 hand about lOh.
ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating agent having a mole ratio of said aromatic compound to the said

aromatic aralkylating agent between about 0.5 and about 50, in the absence or presence of a suitable solvent selected from nitrobenzene, nitromethane and liquid paraffinic hydrocarbons, with a mole ratio of said solvent to said aralkylating agent between about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid catalyst to said aromatic aralkylating agent between about 0.02 and about 2.0 in a stirred batch reactor fitted with a reflux condenser, under vigorous stirring, while bubbling continuously a moisture-free inert gas, such as helium, nitrogen or argon, through the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1 cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the reaction to occur at a temperature between about 25°C and about 300°C at a pressure between about 1 atm and about 10 atm for a reaction period between about 0.01 h and about 50 h, and iii) cooling the reaction mixture to a temperature about 25°C, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art.
The main finding of this invention is that, the said catalyst shows high activity in the aralkylation of aromatic compounds not only when the electron donating group, which is aromatic ring activating group, is present in the aromatic ring to be aralkylated but also when the electron withdrawing group, which is aromatic ring deactivating group, is present in the aromatic ring to be aralkylated, so that the reaction temperature is low and/or the time required for completing the reaction is short.

Other important finding of this invention is that solid catalyst can be reused repeatedly in the aralkylation of said aromatic compounds. Yet another important finding of this invention is that the mechanism of the aralkylation of aromatic compounds over said solid catalyst is different from that of acid catalyzed Friedel-Crafts aralkylation reaction.
Accordingly, the present invention provides an improved process for the preparation of aralkylated aromatic compound, represented by the formula R1R2R3R4QCnH2nC6H3R5R6, having structural formula (1) of the drawing accompanying the specification by the aralkylation of aromatic compound, represented by a the chemical formula R1R2R3R4M, having structural formula (2) of the drawing accompanying the specification with aralkylating agent, represented by a formula R5R6C6H3H2--nX, having structural formula (3) of the drawing accompanying the specification, wherein Q is C6H1 or C10H3 or C14H5; each of R1, R2, R3 and R4 groups is H or CnH2n+1 or CpH2p+1or C6Hs or CnH2n C6Hs or OH or PCnH2n+1 or OC6H5 or halogen or CnH2n+1-xYx or NO2 or NH2 or NHCnH2n+1or N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1 or COCnH2n+1 or SO3H or SO3CnH2n+1or SH or alkyl mercapto group or aryl mercapto group; each of R5 and R6 group of H or CH3 or C2H5 or OH or OCH3 or OC2H5 or NO2 or halogen or NH2 ; X is halogen or OH or SO3H or COOH or OCnH2n+1 or aryl carboxy group or alkyl carboxy group, x is an integer between 1 and 2n+l and n & p are integers greater than or equal to 1 and 2, respectively, and C, H, N, O and S are chemical elements, using a solid catalyst comprising gallium, which comprises:

i) pretreating said solid catalyst at a temperature between 100°C and 800°C in a flow of moisture-free air or inert gas at a gas hourly space velocity in the range 1000 - 2000 cm3 g-1h-1 or under vacuum, for a period between about 0.1 h and about 10 h;
ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating agent having a mole ratio of said aromatic compound to the said aromatic aralkylating agent between 0.5 and 50, in the absence of presence of a suitable solvent selected from nitrobenzene, nitro methane and liquid paraffmic hydrocarbons, with a mole ratio of said solvent to said alkylating agent between about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid catalyst to said aromatic alkylating agent between 0.02 and 2.0 in a stirred batch reactor fitted with a reflux condenser, under vigorous stirring, while bubbling continuously a moisture-free inert gas, such as helium, nitrogen or argon, through the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1 cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the reaction to occur at a temperature between 20°C and 300°C at a pressure between 1 atm and 100 atm for a reaction period between 0.01 h and 50 h, and
iii) cooling the reaction mixture to room temperature, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art.

In the process of the present invention, the preferred reaction temperature is between about 50°C and about 200°C; the preferred reaction pressure is between about 1 atm and about 5 atm; the preferred reaction period is between about 0.05 h and about 20 h; the preferred mole ratio of said aromatic compound to said aralkylating agent is between about 1 and about 20; the preferred weight ratio of said catalyst to said aralkylating agent is between about 0.05 and about 0.5.
In the process of the present invention, a preferred said catalyst is selected from micro or mesoporous gallosilicates and galloaluminosilicates, having structure similar to that of zeolites known in the prior art; Ga+3- exchanged micro and mesoporous zeolites and cationic clays; micro or mesoporous gallophosphatcs or galloaluminophosphates; Ga2O3 and /or Ga-halide impregnated or deposited on micro and mesoporous zeolites, crystalline micro and mesoporous alumino- and metallo- phosphates, cationic and anionic clays, microporous and mesoporous metal oxides or mixed metal oxides and macroporous catalyst supports; gallium oxide pillared clays; and gallium oxide.
A more preferred said catalyst for the process of this invention is selected from H-gallo- and H-galloalumino-silicates of ZSM-5 and MCM-41 type zeolites; Ga2O3 or Ga2O3 deposited on H-ZSM-5 zeolite, MCM-41 zeolite macroporous catalyst supports comprising of silica, alumina, silicon carbide or ZrO2 and HID2 or their mixture; and GaCl3 impregnated on Montmorillonite K10 clay or high silica MCM-41.

The process of this invention can be carried out in a stirred batch reactor, fitted with a reflux condenser and arrangement for bubbling inert gas through the reaction mixture, known in the prior art for carrying out liquid phase reactions.
In the process of this invention, the main products formed are said aralkylated aromatic compound and a by-product HX, wherein H = hydrogen and X = halogen or OH or SO3H or COOH or OCnH2nC6H5 or OCnH2n+1 or arylcarboxy group or alkylcarboxy group, depending upon said aralkylating agent used.
In the process of this invention, said aromatic compound and said aralkylating agent are reactants and are converted partially or completely to said products.
In the process of this invention, the role of said solvent, if used, is to dissolve solid
reactant or reactants, to dilute reactants and/or to facilitate the reaction between said aromatic
compound and said aralkylating agent. However, solvent may not be used in the process of
this invention when both the reactants are liquid at said reaction conditions. Normally, said
solvent is not converted in the process of this invention.
In the process of this invention, the role of inert gas bubbling continuously through the reaction mixture is to remove continuously said by-product from the reaction mixture so that the reverse reaction is avoided or minimised and the time required for completing the reaction is shortened.
In the process of this invention, the role of the reflux condenser fitted with the reactor is to condense reactants and solvents and to return them back to the reaction mixture and allow the inert gas, which is continuously bubbling through the reaction mixture, along with said by-product to escape from the reaction mixture.
In the process of this invention, the reaction pressure above atmospheric pressure may be used to allow the reaction to be carried out at temperature higher than the normal boiling point of the reactants and/or solvent, by increasing the boiling point of said reactants and/or solvent with increasing the reaction pressure.

Said catalyst, used in the process of this invention, is heterogeneous with respect to the reaction mixture and can be removed from the reaction mixture simply by filtration and the removed catalyst, after washing with solvent or said liquid aromatic compound which is to be aralkylated, can be reused in the said process.
Said pretreatment to said catalyst in step-i of the process of present invention is necessary for removing moisture adsorbed on the catalyst so that the catalyst shows its full efficiency for catalysing the reaction between said aromatic compound and said aralkylating agent.
The role of gallium compound present in said catalyst is to activate both the reactants, said aromatic compound and said aralkylating agent. The R5R6C6H3CnH2n----X bond of said aralkylating agent is weakened by its interaction with said gallium compound, leading to the formation of a stable carbocation [R5R6C6H3CnH2nr (I) and X~ . In the presence of said carbocation (I), said aromatic compound is activated on gallium compound by weakening its bond between aromatic nucleus and H, leading to the formation of a penta-coordinated carbocation by the combination of said activated aromatic compound and said carbocation (I). The said penta-coordinated carbocation is then decomposed to said aralkylated aromatic compound, the main product of the reaction, and a proton, which combines with X~ to give HX, the by-product of the reaction.
Said catalyst used in the process of invention can be prepared by various methods, such as hydrothermal synthesis, impregnation, coating, cation exchange, coprecipitation and pillaring of clays, all known in the prior art.

Zeolites are crystalline aluminosilicates containing well defined channels or pores of uniform diameter. A large number of microporous zeolites, such as X, Y, mordenite, L, beta, ZSM-5, ZSM-8, ZSM-11, etc., and mesoporous zeolites, such as M41S type material, e.g. MCM-41, are known in the prior-art. [ ref. Breck in Zeolite Molecular Sieves, Wiley-Interscience Publ., New York, 1974; Beck and Co-workers. J.Am.Chem.Soc., vol.114, page 10834,year 1992; Nature (London) vol.359, page 710, year 1992].
In general, micropores have diameter below 1 run; mesopores have diameter between about 1 nm and about 20 nm; and macropores have diameter above about 20 nm. Said catalyst containing only micropores may be used in the process of this invention when both the reactants have minimum molecular diameter or critical size less than 0.7 nm. Whereas said catalyst containing meso and/or macropores may be used in the process of this invention for both small and large molecular size reactants.
By the process of this invention, benzene, nitrobenzene (which contains highly deactivating electron withdrawing group NCh) and anthracene can be benzylated with benzyl chloride to corresponding aralkylated aromatic compound with a benzyl chloride conversion of 95%, 95% and 95%, respectively, at 1 atm pressure, temperature 80°C, 135°C and 130°C, respectively and reaction period 0.16 h, 0.27 h and 0.31 h, respectively, using Ga2O3 (10 wt %) supported on commercial low surface area ( The present invention is described with respect to the following examples illustrating the process of this invention for the preparation of aralkylated aromatic

compounds. These examples are provided for illustrative purposes only and are not to be construed as limitations on the process of this invention.
Definition of terms used in the examples
Conversion of reactant (%) = mole % of the reactant converted to all products. All the ratios of said aromatic compounds to said aralkylating agent and of said solvent to said aralkylatying agent are mole ratios. The said catalyst to the said aralkylating agent ratio is weight ratio.
The flow rates of gases are measured at 0°C and 1 atm pressure. Gas hourly space velocity (GHSV) is volume of gas, measured at 0°C and 1 atm pressure, passed over unit mass of catalyst per hour.
Ac and Aa represent aromatic compound to be aralkylated and aralkylating agent, respectively.
The micropores, mesopores and macropores have pore diameter of below 1.0 nm, between about 1.0 nm and about 20 nm, and above about 20 nm, respectively.

EXAMPLE-1
This example illustrates the process of this invention for the benzylation of benzene, nitrobenzene, m-xylene, p-xylene, durene (1,2,4,5 tetramethylbenzene ), napthalene and anthracene by benzyl chloride or benzyl bromide to the corresponding benzylated aromatic compounds , using Ga2O3 supported on a commercial macroporous silica alumina (SA 5205) catalyst carrier as a catalyst.
The supported Ga2O3catalyst, Ga203 (10 wt. %)/SA 5205, was prepared by depositing the required amount of gallium nitrate from its aqueous solution on the commercial support SA 5205 (obtained from M/s. NORTON Co. U.S.A.), having main chemical composition : 11.8 % Si02 , 86.1 % A1203 ; surface area
The catalytic benzylation reaction over the Ga2O3 / SA 5205 was carried out by i) pretreating the catalyst in a quartz tubular reactor under a flow of moisture-free
helium at a gas hourly space velocity of 18,000 cm 3 g-1' h-1 at 400 °C for 1 h ,and
then ii) contacting said pretreated catalyst with 15 cm3 liquid reaction mixture containing
aromatic compound to be benzylated and the benzylating agent and optionally a solvent, in a stirred batch reactor (capacity : 50 cm3) fitted with a reflux condenser, mercury thermometer dipped in the reaction mixture and an inlet tube for passing gas through the reaction mixture, under vigorous stirring, while bubbling moisture-free N2 gas through the reaction mixture at the reaction

conditions given in TABLES-1 and 2 and following the course of the reaction by measuring quantitatively the HC1 or HBr evolved during the reaction by absorbing it in aqueous NaOH solution by a simple acid-base titration using phenolphthalein indicator, and
iii) cooling the reaction mixture to room temperature (25°C) and analysing the products and unconverted reactants present in the reaction mixture, after separating the solid catalyst from it by filtration, using chromatographic technique. The results are included in TABLES-1 and 2.

TABLE-1 : Reaction conditions and results of the aralkylation of different aromatic compounds over Ga203(10 wt%)/SA 5205 catalyst.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
TABLE-2 : Reaction conditions and results of the aralkylation of different aromatic compounds over Ga2O3(10 wt%)/SA 5205 catalyst.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
EXAMPLE-2
This example illustrates the process of this invention for the benzylation of benzene and different substituted benzenes by benzyl chloride or benzyl alcohol, as an aralkylating agent, to corresponding benzylated aromatic compounds, using ZSM-5 type microporous H-galloalumino silicate, as a catalyst, in powder form.
The ZSM-5 type H-galloalumino silicate, having Ga/Al = 3, Si/(Al+Ga) = 11.7, and degree of H+ exchange >98% and crystal size = 4-6µm, was prepared by the procedure known in the prior art [ref. Choudhary et al., Journal of Catalysis, vol. 158, page 23 and year 1996; Zeolites vol. 18, page 274 and year 1997 ].
The catalytic benzylation of benzene and substituted benzenes by benzyl chloride or benzyl alcohol over the H-galloalumino silicate catalyst was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLES-3 and 4. The results are included in TABLES-3 and 4.

TABLE-3 : Reaction conditions and results of the aralkylation of different aromatic compounds over a solid catalyst, H-galloalumino silicate of ZSM-5 type.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
TABLE-4 : Reaction conditions and results of the aralkylation of different aromatic compounds over a solid catalyst, H-galloalumino silicate of ZSM-5 type.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
EXAMPLE 3
This example illustrates the process of this invention for the preparation of benzyl benzene and benzyl toluene by benzylation of benzene and toluene, respectively, with benzyl chloride in the absence of any solvent, over H-gallosilicate of ZSM-5 type , as a catalyst, in the form of powder.
The H-gallosilicate (ZSM-5 type), having Si/Ga=33 and degree of H+ exchange >95%and crystal or particle size = 5-6 µm, was prepared by the procedure described earlier [ref. Choudhary et al., Journal of Catalysis, volume 158, page 34 and year 1996 ]. The catalytic benzylation of benzene and toluene by benzyl chloride over H-gallosilicate catalyst was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLE-5, except that the catalyst pre-treatment was carried out under vacuum (2 torr pressure ) at 600°Cfor 0.5 h. The results are included in TABLE-5.

TABLE-5 : Reaction conditions and results of the aralkylation of benzene and toluene over H-gallo'silicate of ZSM-5 type, as a catalyst.

(Table Removed)
Ac = Aromatic compound, Aa - Aralkylating agent
EXAMPLE-4
This example illustrates the process of this invention for the preparation of aralkylated benzene by the aralkylation of benzene with different aralkylating agents, using Ga203 (obtained from M/s Aldrich Chemicals, U.S.A.) and Ga2O3 supported on microporous H-ZSM-5 and silica gel, micro and mesoporous y-Al2O3 and mesoporous high silica MCM-41, as catalysts, in the absence of any solvent.
The Ga2O3 (3.0 wt.%)/H-ZSM-5, Ga203 (10 wt.%)/SiO2 gel, Ga2O3 (10 wt.%)/ y-Al2O3 and Ga2O3 (10 wt.)/highsilica MCM-41 catalysts were prepared by depositing the required amount of gallium nitrate from its aqueous solution on H-ZSM-5 (Si/Al =35.0, degree of H+ exchange >99.0 % and crystal size 3-5 jam), silica gel (Fuji Davison, A-type, surface area 720 m2g-1), y-Al203 (surface area 155 m2g-1) and high silica MCM-41 [prepared by the procedure described in the ref. Choudhary et al., Proceeding of Indian Academy of Sciences, (Chemical Sciences) volume 109, page 229 and year 1997], respectively, in powder form, by incipient wetness technique, drying the impregnated mass at 120°C for 10 h and calcining at 500°C for 6 h.
The catalytic aralkylation of benzene by different aralkylating agents over each of the above catalysts was carried out by the procedure same as that described in EXAMPLE-1 at the reaction conditions given in TABLE-6, except that in the present case the pretreatment of the catalyst was carried out in the flow of moisture-free N2 at 500°C at a gas hourly space velocity of 3000 cm3 .g-1.h11 for 2 h. The results are included in TABLE-6.
The results in TABLE-6 show that the Ga2O3 and supported Ga2O3 catalysts except Ga203./ γ-Al203) show high activity in the benzylation of benzene. However, it
may be noted that the support alone, i.e. H-ZSM-5 zeolite, silica gel, γ- alumina and high silica MCM-41 zeolite, showed no activity in the benzylation of benzene at the said reaction conditions.

TABLE-6 : Reaction conditions and results of the aralkylation of benzene over Ga203 supported on different catalyst carriers, as a catalyst.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
EXAMPLE-5
This example illustrates the process of this invention for the benzylation of benzene and substituted benzenes by benzyl chloride to corresponding benzylated aromatic compounds, using GaCl3 impregnated Montmorillonite K10 clay catalyst in the absence of a solvent.
The GaCl3 (10 wt.%)/MontmoriIlonite K10 clay catalyst was prepared by impregnating required amount of GaCl3 from its dry acetonitrile solution on Montmorillonite K10 clay (obtained from Aldrich Chemicals co. U.S.A.) in powder form, following the incipient wetness technique and drying the impregnated mass at 60°C under vacuum for 10 h.
The catalytic benzylation of benzene and substituted benzenes by benzyl chloride over the above catalyst has been carried out by the procedure same as that described in EXAMPLE-1, at the reaction conditions given in TABLE-7, except that in the present case the pretreatment of the catalyst was carried out at 120 °C in the flow of moisture-free helium gas at a gas hourly space velocity of 6000 cmjg -1 h-1 for 5 h. The results are included in TABLE-7.

TABLE-7 : Reaction conditions and results of the aralkylation of different aromatic compounds over GaCl3/Montmorillonite K1Q, as a catalyst.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
EXAMPLE-6
This example illustrates the process of this invention for the benzylation of toluene by benzyl chloride using Ga2O3/SA 5205 catalyst prepared in EXAMPLE-1, and reused of this catalyst for the subsequent reactions carried out in a number of batches. The benzylation reactions was carried out using the Ga2O3/SA 5205 catalyst, prepared in EXAMPLE-1, and by the procedure same as that described in EXAMPLE-1, at the reaction conditions given in TABLE-8, except that in the present case the catalyst used in the second and onward batches was not given said pretreatment, Instead the catalyst obtained by filtration from the reaction mixture of first batch was used as it is, after washing it with toluene, for the second batch reaction, and so on. The results are given in TABLE-8. The results show that the catalyst can be reused repeatedly for the process.

TABLE-8 : Reaction conditions and results of the aralkylation of toluene by benzyl chloride over Ga2O3(10 wt%)/SA 5205 catalyst, fresh and reused in the subsequent batches.

(Table Removed)
Ac = Aromatic compound, Aa = Aralkylating agent
The main advantages of the process of this invention over the prior art processes for the preparation of aralkylated aromatic compounds are as follows:
1) The process of this invention has a number of advantages over the earlier homogeneous catalysed processes for the preparation of aralkylated aromatic compounds, as follows: In the process of this invention i) the catalyst used is heterogeneous solid catalyst and hence it can be separated
T
from the reaction products simply by filtration ,
ii) the separated catalysts can be reused in the process for a number of times, and iii) also the catalyst is non corrosive, therefore most of the serious problems associated with homogeneous catalyst used in the earlier homogeneous catalysed processes for the preparation of aralkylated aromatic compounds are overcome m the process of this invention. 2) The process of this invention has also number of advantages over the prior art
processes based on the use of solid catalyst for the preparation of aralkylated
aromatic compounds, as follows:
i) The activity of the said catalyst used in the process of present invention is
higher.
ii) The process of the present invention can be used for aralkyating both small and
large size aromatic compounds with both small and large size aralkylating agents
to produce the corresponding aralkylated compounds.
iii) In the process of this invention, since moisture-free inert gas is bubbled
through the reaction mixture continuously, said by-product formed in the reaction
is removed continuously and thereby the reverse aralkylation reaction is avoided or minimised, thus requiring shorter time for completing the reaction, iv) In the process of this invention, it is possible to carry out the aralkylation reaction at a temperature higher than the normal boiling point of either of the reactants and the solvent, and thereby the reaction period for completing the reaction is shortened and/or the inhibition of the reaction due to strong adsorption of the reactants, products or solvent on the catalyst is avoided or minimised, v) By the process of this invention, the aralkylation of said aromatic compound is possible at mild reaction conditions even though when the aromatic compound does not contain any aromatic nucleus activating group or electron donating group, for example when aromatic compound is benzene, or when said aromatic compound contains electron withdrawing group, for example halide or nitro group, which has highly deactivating effect on the aromatic nucleus for the aralkylation reaction.

We Claim:
1. An improved process for the preparation of aralkylated aromatic compound, represented
by a general chemical formula: RiR2R3R4QCnH2nC6H3R5R6, having structural formula
(1) of the drawing accompanying the specification by the aralkylation of aromatic
compound, represented by a general chemical formula R1R2R3R4M, having structural
formula (2) of the drawing accompanying the specification with aralkylating agent,
represented by a general chemical formula : R5R6C6H3H2nX, having structural formula
(3) of the drawing accompanying the specification wherein Q is C6H1 or C10H3 or C14H6;
each of R1, R2, R3 and R4 groups is H or CnH2n+1 or CpH2p-1 or CeHs or CnH2n C6H5 or
OH or PCnH2n+, or OC6H5 or halogen or CnH2n+1xYx or NO2 or NH2 or NHCnH2n+1or
N(CnH2n+1)2 or NHCOCnH2n+1 or NHCOC6H5 or CN or CHO or COOH or COOCnH2n+1
or COCnH2n+1 or SO3H or SO3CnH2n+1 or SH or alkyl mercapto group or aryl mercapto
group; each of R5 and R6 group of H or CH3or C2H5 or OH or OCH3 or OC2H5or NO2
or halogen or NH2; X is halogen or OH or SO3H or COOH or OCnH2n+1 or aryl carboxy
group or alkyl carboxy group, x is an integer between 1 and 2n+l and N & P are integers
greater than or equal to 1 and 2, respectively, and C, H, N, O and S are chemical
elements, using a solid catalyst comprising gallium, which comprises:
i) pretreating said solid catalyst at a temperature between 100°C and 800°C in a flow of
moisture-free air or inert gas at a gas hourly space velocity in the range 1000 - 2000
cm3 g-1h-1or under vacuum, for a period between about 0.1 h and about 10 h
ii) contacting a liquid mixture of said aromatic compound and said aromatic aralkylating
agent having a mole ratio of said aromatic compound to the said aromatic
aralkylating agent between 0.5 and 50, in the absence of presence of a suitable
solvent selected from nitrobenzene, nitro methane and liquid paraffmic
hydrocarbons, with a mole ratio of said solvent to said alkylating agent between
about 0 and about 50 with said pretreated solid catalyst at a weight ratio of solid
catalyst to said aromatic alkylating agent between 0.02 and 2.0 in a stirred batch
reactor fitted with a reflux condenser, under vigorous stirring, while bubbling
continuously a moisture-free inert gas, such as helium, nitrogen or argon, through
the said liquid reaction mixture containing the said catalyst at a flow rate above 0.1
cm3 of inert gas per cm3 of liquid reaction mixture per minute and allowing the
reaction to occur at a temperature between 20°C and 300°C at a pressure between 1
atm and 100 atm for a reaction period between 0.01 h and 50 h, and

iii) cooling the reaction mixture to room temperature, removing said catalyst from the reaction mixture by filtration and then separating the reaction products from the reaction mixture by the methods known in the prior art.
2. An improved process as claimed in claim 1, wherein the reaction temperature is between
50°C and 200°C.
3. An improved process as claimed in claim 1, wherein the reaction pressure is between 1.0
atm to 5.0 atm.
4. An improved process as claimed in claim 1, wherein the reaction period ranges between
0.05 h and 20h.
5. An improved process as claimed in claim 1, wherein the mole ratio of said aromatic
compound to said aralkylating agent is between 1 and 20.
6. An improved process as claimed in claim 1, wherein a weight ratio of said catalyst to
said aralkylating agent is between 0.05 to 0.5.
7. An improved process as claimed in claim 1, wherein said catalyst is selected from micro
or mesoporous Gallo silicates and galloaluminosilcates, having structure similar to that
of zeolites; Ga+3 - exchanged micro and mesoporous zeolites and cationic clays; miro or
mesoporous gallophosphates or galloaluminophosphates; Ga2O3 and/or Ga-halide
impregnated or deposited on micro and mesoporous zeolites, crystalline micro or
mespoporous alumino-, silico-alumino and metallophosphates, cationic and anionic
clays, micro porous and mespoporous metal oxides or mixed metal oxides and
macroporous ctalyst supports; and gallium oxide pillared clays; and gallium oxide.
8. An improved process as claimed in claims 1 and 7, wherein said catalyst is selected from
-gallo-and H-galloalumino-silicated of ZSM-5 zeolite, MCM-41 zeolite and
macroporous catalyst supports comprising of silica, alumina, silicon carbide or ZrO2 and
HfO2 or their mixture; and GaCl3 impregnated on Montmorillonite K10 clay or high
silica MCM-41.
9. An improved process for the preparation of aralkylated aromatic compound using solid
catalyst comprising of gallium, substantially as herein described with reference to the
examples.

Documents:

2877-del-1998-abstract.pdf

2877-del-1998-claims.pdf

2877-del-1998-correspondence-others.pdf

2877-del-1998-correspondence-po.pdf

2877-del-1998-description (complete).pdf

2877-del-1998-drawings.pdf

2877-del-1998-form-1.pdf

2877-del-1998-form-19.pdf

2877-del-1998-form-2.pdf

2877-del-1998-form-3.pdf

2877-del-1998-petition-138.pdf

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Patent Number

215038

Indian Patent Application Number

2877/DEL/1998

PG Journal Number

10/2008

Publication Date

07-Mar-2008

Grant Date

20-Feb-2008

Date of Filing

25-Sep-1998

Name of Patentee

COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH

Applicant Address

RAFI MARG, NEW DELHI-110 001, INDIA

Inventors:

#	Inventor's Name	Inventor's Address
1	DR. VASANT RAMACHANDRA CHOUDHARY	NATIONAL CHEMICAL LABORATORY, PUNE-8, INDIA.
2	MR. SUMAN KUMAR JANA	NATIONAL CHEMICAL LABORATORY, PUNE-8, INDIA
3	MR. B-PHANI KIRAN	NATIONAL CHEMICAL LABORATORY, PUNE-8,INDIA

PCT International Classification Number

C07C 41/06

PCT International Application Number

N/A

PCT International Filing date

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1			NA