Title of Invention

"A PROCESS FOR THE MANUFACTURE OF 1,1,1,3,3-PENTAFLUOROPROPANE"

Abstract

This invention is related to the preparation of hydrofluorocarbons (HFCs). Specifically, it relates to the fluorination of a compound of the formula: CFyCl3-yCH2CHFwCl2-w wherein w = 0 or 1, and y = 0 - 3, with hydrogen fluoride in the presence of a fluorination catalyst under conditions sufficient to produce a compound of the formula CF3CH2CF2H. CF3CH2CF2H or HFC 245fa may be used as a blowing agent, a propellant, and a heat transfer agent.

Full Text

PROCESS FOR THE MANUFACTURE OF 1.1,1.3.3-PENTAFLUOROPROPANE BACKGROUND OF THE INVENTION This invention relates to a novel method of manufacturing 1,1,1,3,3-pentafluoropropane, CF3CH2CF2H, which is referred to in the art as HFC-245fa. Specifically, the invention relates to the fluorination with hydrogen fluoride of a compound of the formula: CFyCl3.yCH2CHFwCl2.w wherein w = 0 or 1, and y = 0 - 3, in the presence of a fluorination catalyst to produce HFC-245fa. HFC-245fa has physical properties, including a boiling point of about 14 °C , which make it particularly attractive as a blowing agent. (See Ger. OflFen, DE 3,903,336, 1990 (EP 381,986 A)). It also has the ability to function as an aerosol propellant (U.S. Patent 2,942,036 to Smith and Woolf) in a manner similar to trichlorofluoromethane, which is referred to in the art as CFC-11, and as a heat transfer agent. (Jpn. Kokai Tokyo Koho JP 02,272,086 in 114 Chemical Abstracts 125031q(1991)). Traditionally, chlorofluorocarbons (CFCs) like CFC-11 and dichlorodifluoromethane (CFC-12) have been used as refrigerants, blowing agents and propellants. These materials, however, are believed to contribute to stratospheric ozone depletion. The fluorocarbon industry therefore has focused its attention on developing stratospherically safer alternatives to these materials. HFC-245fa is a candidate replacement material since it fijnctions in substantially the same way as the CFCs but is zero ozone depleting. Because the demand for these and other low or zero ozone depleting materials will increase dramatically in the fijture, commercially viable processes for their preparation are needed. Only two methods for manufacturing HFC-245fa (which are not hydrofluorination reactions) are reported in the art. However, these methods are not without their shortcomings. Knunyants, et al.. Catalytic Hydrogenafion ofPerfliioro Olefins , 55 Chemical Abstracts 349f (1961), discloses the reduction of 1,1,1,3,3-pentafluoropropene to HFC-245fa. Because this process includes multiple steps, it is inefficient and uneconomical. Burdon, et al.. Partial Fluoridation of Tetrahydrqfiiran with Cobalt Trifluoride, J. Chem. Soc. (C), 1739 (1969), discloses the elemental fluorination of tetrahydrofliran to produce HFC-245fa, This process suffers the disadvantage that it produces a host of other by-products, thus reducing the yield of the desired product. As far as hydrofluorination reactions are concerned, there are no such methods for the production of HFC-245fa reported in the art, let alone fluorination reactions which use 1,1,1,3,3-pentachloropropane (CCI3CH2CHCI2) as the starting material to produce HFC-245fa. Although the conversion of-CCI3 groups to -CF3 groups is well-known in the art, attempts to fluorinate terminal -CHCI2 or -CHCIF groups to -CHF2 groups in compounds having more than two carbons, (in particular compounds of the formula RCH2CHCI2 and RCH2CHnFX wherein X is CI or Br and R is an alkyl group having at least one carbon atom), have not been successful. See Henne, et al., Fluoroethanes andFhioroethy/enes, 58 J. Am. Chem. Soc. 889 (1936). Tarrant, et al., Free Radical Additiom Involving Fluorine Compounds. IV. The Addition of Dibromodifluoromethane to Some Fluoroolefins, 11 J. Am. Chem. Soc. 2783 (1955) report the fluorination of compounds of the type CF2BrCH2CHFBr with hydrogen fluoride (HF) in the presence of a Sb(V) salt catalyst, such as SbCl5 andTaFf. However, this method produced only a 14% yield of CF3CH2CHFBr at 125°C, and only a modest improvement in yield at 170°C. Even at elevated temperatures, no HFC-245fa was produced. DESCRTPTION OF THE INVENTION We have discovered that the drawbacks associated with the prior art processes for manufacturing 1,1,1,3,3-pentafluoropropane or HFC-245fa can be eliminated by the process of our invention. That is, we have discovered an efficient and economical means of manufacturing HFC-245fa on a commercial scale, which uses readily available raw materials and which produces HFC-245fa in high yield. The invention relates to a process for manufacturing 1,1,1,3,3-pentafluoropropane comprising: 1) reacting a compound of the formula: CFyCl3-yCH2CHFwCl2-w wherein w = 0 or 1, and y = 0 - 3, with hydrogen fluoride in the presence of a fluorination catalyst under conditions sufficient to produce a compound of the formula CF3CH2CF2H; and 2) optionally recovering a compound of the formula CF3CH2CF2H. The organic starting materials corresponding to the formula CFyCl3. yCH2CHFwCl2-w , wherein w = 0 or 1, and y = 0 - 3, include CCI3CH2CHCI2, CF3CH2CHCI2, CFCI2CH2CHCI2, CF2CICH2CHCI2, CFCI2CH2CHCIF, CF2CICH2CHFCI, and CF3CH2CHFCI. The preferred starting material is CCI3CH2CHCI2. These materials are not commercially available. However, they may be prepared by any means well-known in the art. See, for example, B. Boutevin, et al., Monofimctional Vinyl Chloride Telomers. I. Synthesis and Characterization of Vinyl Chloride Telomer Standards, 18 Eur, Polym. J. 675 (1982) in 97 Chemical Abstracts 182966c (1982); and Kotora, et al.. Selective Additions of Polyhalogenated Compounds to Chloro Substituted Elhenes Catalyzed by a Copper Complex, 44(2) React. Kinet. Catal. Lett. 415 (1991). See also the method disclosed in Examples 1 and 2 below. When CCI3CH2CHCI2 is the starting material, it is preferably prepared according to the method provided in Example 1 below. Alternatively, CCI3CH2CHCI2 may be prepared by the reduction of CCI3CH2CCI3 (see Example 2) as well as by photochlorination of CCI3CH2CH2CI. Any water in the HF will react with and deactivate the fluorination catalyst. Therefore, substantially anhydrous HF is preferred. By "substantially anhydrous" we mean that the HF contains less than about 0.05 weight % water and preferably contains less than about 0.02 weight % water. However, one of ordinary skill in the art will appreciate that the presence of water in the catalyst can be compensated for by increasing the amount of catalyst used. HF suitable for use in the reaction may be purchased from AlliedSignal Inc. of Morristown, New Jersey. Based on reaction stoichiometry, the required mole ratio of HF to organics (i.e., CFyCl3-yCH2FwCl2-w) 's 5-y-w (or the number of chlorine atoms in the organic starting material) to 1.0. HF is preferably used in an amount from about 1 to about 15 times the stoichiometric amount of HF to organics, and more preferably from about 6 to about 15 times the stoichiometric amount of HF to organics. Fluorination catalysts useful in the process of the invention include; (I.) pentavalent antimony, niobium, arsenic and tantalum halides; (II.) pentavalent antimony, niobium, arsenic and tantalum mixed halides; and (III.) mixtures of pentavalent antimony, niobium, arsenic and tantalum halide catalysts. Examples of catalysts of group (I.) include antimony pentachloride and antimony pentafluoride. Examples of catalysts of group (II.) include SbCl2F3 and SbBr2F3. Examples of catalysts of group (III.) include a mixture of antimony pentachloride and antimony pentafluoride. Pentavalent antimony, niobium, arsenic and tantalum halides are commercially available, and mixed halides thereof are created in situ upon reaction with HF. Antimony pentachloride is preferred because of its low cost and availability. Pentavalent antimony mixed halides of the formula SbClnF5_n where n is 0 to 5 are more preferred. The fluorination catalysts used in this invention preferably have a purity of at least about 97%. Although the amount of fluorination catalyst used may vary widely, we recommend using from about 5 to about 50%, or preferably from about 10 to about 25% by weight catalyst relative to the organics. It may be advantageous to periodically regenerate the catalyst due to the dissociation of the pentavalent catalyst over time. This may be accomplished by any means well known in the art. The catalyst may be regenerated, for example, by adding chlorine (in an amount of from about 1 to about 10 mole percent relative to the amount of pentavalent catalyst initially present in the reactor) to the combination stream comprised of organics of the formula CFyCl3-yCH2CHFYwCl2-w, and the recycled stream comprised of under-fluorinated materials and HF. The chlorine, which is continuously added to the process of this invention when operating in a continuous mode (and periodically added when operating in a batch mode), oxidizes the catalyst from the trivalent to the pentavalent state. One of ordinary skill in the art can readily determine without undue experimentation the amount of chlorine to be added in order to optimize the use of the catalyst. The temperature at which the fluorination reaction is conducted and the period of reaction will depend on the starting material and catalyst used. One of ordinary skill in the art can readily optimize the conditions of the reaction without undue experimentation to get the claimed results, but the temperature will generally be in the range of from about 50 to about 175 °C, and preferably from about 115 to about 155 °C, for a period of, for example, from about 1 to about 25 hours, and preferably from about 2 to about 8 hours. Pressure is not critical. Convenient operating pressures range from about 1500 to about 5000 KPa, and preferably from about 1500 to about 2500 KPa. The equipment in which the fluorination reaction is conducted is preferably made of corrosion resistant material such as Inconel or Monel. HFC-245fa may be recovered from the mixture of unreacted starting materials, by-products, and catalyst by any means known in the art, such as distillation and extraction. As illustrated in Example 3, at the end of the heating period, i.e. the amount of time for complete reaction in batch mode operations, the fluorination reaction product and remaining HF may be vented through a valve on the autoclave head, which in turn is connected to an acid scrubber and cold traps to collect the product. Alternatively, unreacted HF and organics may be vented and condensed, and the HF layer recycled to the reactor. The organic layer can then be treated, i.e. washed with an aqueous base, to remove dissolved HF and distilled. This isolation procedure is particularly useful for a continuous fluorination process. Under-fluorinated materials, such as CF3CH2CHFCI, may be recycled in subsequent runs. In another embodiment, the invention relates to a process for the manufacture of 1,1,1,3,3-pentafluoropropane which comprises: 1. reacting CCI4 and vinyl chloride in the presence of a telomerization catalyst under conditions sufficient to produce a compound of the formula CCI3CH2CHCI2; 2. reacting a compound of the formula CCI3CH2CHCI2 with hydrogen fluoride in the presence of a fluorination catalyst under conditions sufficient to produce a compound of the formula CF3CH2CF2H; and 3. optionally recovering a compound of the formula CF3CH2CF2H. The telomerization of vinyl chloride by reaction with carbon tetrachloride to produce CCI3CH2CHCI2 is known in the art. See, for example, B. Boutevin, et al., Monofimctional Vinyl Chloride Telomers. I. Synthesis and Characterization of Vinyl Chloride Telomer Standards, 18 Eur. Polym. J. 675 (1982) in 97 Chemical Abstracts 182966c (1982); and Kotora, et al.. Selective Additions of Polyhalogenated Compounds to Chloro Substituted Elhenes Catalyzed by a Copper Complex, 44(2) React. Kinet. Catal. Lett. 415 (1991). The starting materials for the telomerization reaction, i.e. carbon tetrachloride and vinyl chloride, are available from commercial sources. The molar ratio of CCI4 to vinyl chloride is about 0.5:10, preferably about 1:8 (in order to minimize the formation of higher telomers), and most preferably about 1:5. The telomerization of vinyl chloride can be initiated by any commercially available catalyst known in the art to be useful in initiating and catalyzing the telomerization of carbon tetrachloride and vinyl chloride. Suitable catalysts include, but are not limited to, organic peroxides, metallic salts, and metal carbonyls. Copper and iron salt catalysts, such as cuprous chloride (CuCI), cuprous iodide (Cul), and iron chloride (FeCl2), are preferred. The amount of catalyst used in the telomerization reaction is at least about 0.1 to about 50 mmol, and preferably about 1 to about 20 mmol per mole of organics (i.e., CCI3CH2CHCI2). An amine co-catalyst, such as an alkanol amine, alkyl amine, and aromatic amine, may optionally be used in order to allow for the use of milder conditions in the telomerization process. Examples of suitable amine co-catalysts include ethanol amine, butyl amine, propyl amine, benzylamine, and pyridine. 2-propylamine is the most preferred co-catalyst. Such co-catalysts are commercially available. When a co-catalyst is used, it should be used in an amount from about 1 to about 10 moles per mole of catalyst, i.e., e.g. copper salt. In order to dissolve the catalyst, a solvent, which is inert to the reactants and the desired product, may be used in the telomerization reaction. Suitable solvents include, but are not limited to, commercially available acetonitrile, dimethylsulfoxide, dimethylformamide, tetrahydrofuran, isopropanol, and tertiary butanol. Acetonitrile is preferred because of ease of handling and stability. The amount of solvent used ranges from about 5 times the amount of catalyst used on a mole basis to about 80 percent of the total volume of the total telomerization reaction mixture (i.e., solvent, catalyst, co-catalyst, carbon tetrachloride, vinyl chloride), and more preferably between about 10 to 50 times the amount of catalyst used on a mole basis. The temperature at which the telomerization reaction is conducted and the period of reaction will depend on the catalyst selected, the presence of a co-catalyst, and the solubility of the catalyst system in the solvent. One of ordinary skill in the art can readily optimize the conditions of the reaction without undue experimentation to get the claimed results but the temperature will generally be in the range of from about 25 to about 225 °C, preferably from about 50 to about 150 °C. The period of reaction will generally range from about 3 to about 72 hours, preferably from about 10 to about 24 hours. Pressure is not critical. Preferably the telomerization reaction is conducted in a conventional apparatus, such as an autoclave made of corrosion resistant materials such as Teflon and glass. Preferably, the telomerization product is recovered from by-products, solvent, catalyst and co-catalyst prior to the fluorination reaction to substantially eliminate the production of by-products in the fluorination step. The telomerization product may be recovered by any means well known in the art such as distillation and extraction. Optionally, the telomerization product may be further purified by additional distillation. Due to the toxicity of vinyl chloride, other procedures for preparing CCI3CH2CHCI2 may be employed. See Example 2 (reduction of CCI3CH2CCI3). Alternatively, CCI3CH2CCI3 may be prepared according to the well-known telomerization reaction of vinylidene chloride with carbon tetrachloride. Example 1. Preparation of CCl3CH2CHl2 from CCl4 and CH2=CHCl A 600-mL monel autoclave equipped with mechanical stirrer was charged with 1 g CuCl, 156.6 g CCI4 and 75 mL acetonitrile. The contents were cooled in an ice bath, and the autoclave was closed and evacuated briefly. 36.7 g of vinyl chloride was then added, and the contents stirred and heated to 135 °C for 16 hours. The volatile materials were removed by distillation at atmospheric pressure. Distillation at 23 mm Hg resulted in 90.0 g (71% yield based on vinyl chloride added) of a colorless liquid. The identity of this liquid was confirmed via proton nuclear magnetic resonance ("NMR") to be CCI3CH2CHCI2 (boiling point 72-74 °C. ^H NMR (CDCI3): 5 6.15 (t, lH),3.7(d,2H)). Example 2. Preparation of CCl3CH2ChCl2 by reduction of CCl2CH2CCl3 A 600-mL monel autoclave equipped with mechanical stirrer was charged with 199.9 g CCI3CH2CCI3, 199.5 g isopropanol, and 4 g Cul. The autoclave was closed and evacuated briefly. The contents were heated to 120 - 125 °C for 16 hours. The volatile materials, including by-product isopropyl chloride, were removed by rotary evaporation, leaving 200 g of residue . Analysis on a Varian gas chromatograph having a packed column ("GC Analysis") indicated CCl3CH2CHCl2 and CCI3CH2CCI3 in a ratio of about 1;2, respectively. Distillation at 29 mmHg resulted in 107.9 g of starting material (boiling point from about 105 to 107 °C), and 36.9 g (46% yield) of CCI3CH2CHCI2 (boiling point from about 85 to 90 °C). Example 3. Fluorination of CCl3CH2CHCI2 with HF/SbCIg A 600-mL monel autoclave equipped with mechanical stirrer was charged with 8.7 g SbCl5 and cooled to -27 ° C. The autoclave was then evacuated and charged with 49.8 g of anhydrous HF. The contents were cooled to -40 ° C, and 44 g CCI3CH2CHCI2 was added. The reactor was then connected to a packed column/condenser assembly. The condenser was maintained at -20 °C. The reaction mixture was heated to 135 ° C over 2.25 hours and maintained at that temperature for an additional 2 hours. During this heating period, the pressure in the autoclave was maintained from about 1965 to 2655 KPa (300 - 400 psig) by periodically venting pressure (HCl by-product) in excess of 2655 KPa (400 psig). Venting was done from the top of the condenser to a cold aqueous KOH scrubber which was connected to -78 °C cold trap. The reactor was then completely vented to the cold trap. 18.5 g of a colorless liquid were collected. The identity of this liquid was determined by GC analysis to be 84% CF3CH2CHF2 (corresponding to a yield of 57%) and 1 l%i CF3CH2CHCIF. Example 4. Fluorination of CF3CH9CHCl2 with HF/SbF5; The experiment described in Example 3 was repeated except that CF3CH2CHCI2 was used as the starting material. To the apparatus described in Example 3 was charged 8.2 g SbF5, 41 g HF, and 37 g CF3CH2CHCI2. (The CF3CH2CHCI2 was obtained via the room temperature photochlorination of commercially available CF3CH2CH2CI.) This mixture was heated with stirring to about 130 - 135 °C for 4.5 hours at a maximum operating pressure of 3450 KPa. 18.1 g (corresponding to a yield of 57%)) of a colorless liquid were recovered. GC analysis identified the material as 94%) pure HFC-245fa . Examples. Fluorination of CF3CH2CHCI2 with HF/SbCl5 at 150 - 160 °C and Low Operating Pressure The experiment described in Example 3 was repeated except that CF3CH2CHCI2 was used as the starting material. To the apparatus described in Example 3 was charged 9.5 g SbC15, 47.9 g HF, and 34.6 g CF3CH2CHCI2. This mixture was heated with stirring to about 150 - 160 °C for 3.5 hours and maintained at that temperature for an additional 2 hours. The maximum operating pressure, controlled by periodic venting of by-product HCl, was 1280 KPa. GC analysis of the crude reaction product indicated that it contained 71% HFC-245fa. As illustrated by the above-described Examples, PIFC-245fa is produced in high yield without the use of high temperatures or pressures and without using large quantities of expensive catalysts. WE CLAIM:- 1. A process for the manufacture of 1,1,1,3,3-pentafluoropropane which comprises: a) reacting CCl4 and vinyl chloride under conditions sufficient to produce a compound of the formula CCI3CH2CHCI2; and b) reacting a compound of the formula CCI3CH2CHCI2 with hydrogen fluoride in the presence of a fluorination catalyst to produce a compound of the formula CF3CH2CF2H. 2. The process as claimed in claim 1, wherein said CCI3CH2CHCI2 is recovered prior to step b. 3. A process for the manufacture of 1,1,1,3,3-pentafluoropropane substantially as herein described with reference to the foregoing examples.

Documents:

1575-del-2003-Abstract-(02-07-2013).pdf

1575-del-2003-abstract.pdf

1575-del-2003-Claims-(02-07-2013).pdf

1575-del-2003-claims.pdf

1575-del-2003-Correspondence-Others-(02-07-2013).pdf

1575-del-2003-Correspondence-Others-(11-07-2013).pdf

1575-del-2003-correspondence-others.pdf

1575-del-2003-correspondence-po.pdf

1575-del-2003-description (complete).pdf

1575-del-2003-form-1.pdf

1575-del-2003-form-18.pdf

1575-del-2003-form-2.pdf

1575-del-2003-Form-3-(02-07-2013).pdf

1575-del-2003-Form-3-(11-07-2013).pdf

1575-del-2003-form-3.pdf

1575-del-2003-Form-5-(02-07-2013).pdf

1575-del-2003-form-5.pdf

1575-del-2003-GPA-(02-07-2013).pdf

1575-del-2003-gpa.pdf

1575-del-2003-Petition-137-(11-07-2013).pdf