Title of Invention	"A METHOD FOR THE SYNTHESIS OF SEVERELY STERICALLY HINDERED SECONDRY AMINOETHER ALCOHOLS OF THE FORMULA (I)"
Abstract	A method for the synthesis of severely sterically hindered secondary aminoether alcohols of the formula wherein R1, R2, R3, R5, R6, R7, R8, R9, R10 and R11 are as herein described as in the specification and claims.

Full Text

SYNTHESIS OF SEVERELY STERICALLY HINDERED SECONDARY AMINOETHER ALCOHOLS FROM A KETENE AND/OR CARBOXYLIC ACID HALIDE AND/OR CARBOXYLIC ACID ANHYDRIDE FIELD OF THE INVENTION [0001] The present invention relates to a process for the preparation of severely sterically hindered secondary aminoether alcohols. DESCRIPTION OF RELATED ART [0002] It is well-known in the art to treat gases and liquids, such as mixtures containing acidic gases including CO2, H2$, CS2, HCN, COS and oxygen and sulfur derivatives of CtoC4 hydrocarbons with amine solutions to remove these acidic gases. The amine usually contacts the acidic gases and the liquids as an aqueous solution containing the amine in an absorber tower with the aqueous amine solution contacting the acidic fluid countercurrently. Usually this contacting results in the simultaneous removal of substantial amounts of both the CO2 and H2S. USP 4,112,052, for example, utilizes a sterically hindered amine to obtain nearly complete removal of CO2 and H2S acid gases. This process is particularly suitable for systems in which the partial pressures of the CO2 and related gases are low. For systems where the partial pressure of CO2 is high or where there are many acid gases present, e.g., H2S, COS, CHsSH, CS2, etc., a process utilizing an amine in combination with a physical absorbent, referred to as a "non-aqueous solvent process" is practiced. Such a system is described in USP 4,112,051. [0003] Selective removal of H2S from acid gas systems containing both H2S and CO2, however, is very desirable. Such selective removal results in a relatively high H2S/CO2 ratio in the separated acid gas which facilitates the subsequent conversion of the H2S to elemental sulfur in the Claus process. [0004] The typical reactions of aqueous secondary and tertiary amines with CO2 and H2S can be represented as follows: H2S + R3N « » R3NH+ + HS~ H2S + R2NH « » R2NH2 f + HS~ C02 + R3N + H20 « * R3NH+ + HCO3 CO2 + 2 R2NH « * R2NH2 + R2NCO2 where R is the same or different organic radical and may be substituted with a hydroxyl group. Because the reactions are reversible they are sensitive to the CO2 and H2S partial pressures which is determinative of the degree to which the reactions occur. [0005] Selective H2S removal is particularly desirable in systems having low H2S/CO2 ratios and relatively low H2S partial pressures as compared to that of the CO2. The ability of amine to selectivity remove H2S in such systems is very low. [0006] Solutions of primary and secondary amines such as monoethanolamine (MEA), diethanolamine (DEA), diisopropanolamine (DPA), and hydroxyethoxyethylamine (DEA) absorb both H2S and CO2, and thus have proven unsatisfactory for the selective removal of H2S to the exclusion of CO2- The CO2 forms carbamates with such amines relatively easily. [0007] H2S has been selectively removed from gases containing H2S and C&2 by use of diisopropanolamine (DIPA) either alone or mixed with a nonaqueous physical solvent such as sulfolane. Contact times, however, must be kept short to take advantage of the faster reaction of H2S with the amine as compared to the rate of CO2 reaction with the amine. [0008] Frazier and Kohl, Ind. and Eng. Chem., 42,2288 (1950) showed that the tertiary amine methydiethanolamine (MDEA) is more selective toward H2S absorption as compared to CO2- C(>2 reacts relatively slowly with tertiary amines as compared to the rapid reaction of the tertiary amine with H2S. However, it has the disadvantage of having a relatively low H2S loading capacity and limited ability to reduce the H2S content to the desired level at low H2S pressures encountered in certain gases. [0009] UK Patent Publication No. 2,017,524A discloses the use of aqueous solutions of dialkylmonoalkanolamines, e.g., diethylmonoethanol amine (DEAE), for the selective removal of H2S, such material having higher selectivity and capacity for H2S removal at higher loading levels than MDEA. DEAE, however, has the disadvantage of a low boiling point of 161°C, making it relatively highly volatile resulting in large material loss. [0010] USP 4,471,138 the entire teaching of which is incorporated herein by reference, teaches severely sterically hindered acyclic secondary aminoether alcohols having a high selectivity for H2S compared to CO2. Selectivity is maintained at high H2S and CCO2 loadings. [0011] The severely sterically hindered acyclic aminoether alcohols of USP 4,471,138 are represented by the general formula: (Figure Removed) wherein RI and R2 are each independently selected from the group consisting of alkyl and hydroxyalkyl radicals having 1-4 carbon atoms, R3, R4, RS and Rg are each independently selected from the group consisting of hydrogen, alkyl, and hydroxyalkyl radicals having 1-4 carbon atoms, with the proviso that at least one of R4 or RS bonded to the carbon atom which is directly bonded to the nitrogen atom is an alkyl or hydroxyalkyl radical when R3 is hydrogen, x and y are each positive integers ranging from 2-4, and z is a positive integer ranging from 1-4. These materials are prepared by a high temperature reaction preferably in the presence of a solvent, of a secondary or tertiary alkyl primary amine with an ether alcohol containing a carbonyl functionality hi the presence of a source of hydrogen or with a haloalkoxyalkanol. Preferably the composition is of the general formula: (Figure Removed) [0012] U.S. Patent 4,487,967 is directed to a process for preparing severely sterically hindered secondary aminoether alcohols by reacting a primary amino compound with a polyalkenyl ether glycol in the presence of a hydrogenation catalyst at elevated temperatures and pressures. The primary amino compounds employed have a general formula: where Rl is selected from the group consisting of secondary or tertiary alkyl radicals having 3 to 8 carbon atoms or cycloalkyl radicals having 3 to 8 carbon atoms. The polyalkenyl ether glycols employed have the general formula: (Figure Removed) where R2, RS, R4 and R$ are each independently selected from the group consisting of hydrogen, C1-C4 alkyl radicals, and Cs-Cg cycloalkyl radicals, with the proviso that if the carbon atom of Rj directly attached to the nitrogen atom is secondary, at least one of R2 and R3 directly bonded to the carbon which is bonded to the hydroxyl group is as alkyl or cycloalkyl radical, x and y are each positive integers independently ranging from 2 to 4 and z is from 1 to 10, preferably 1 to 6, more preferably 1 to 4. The process is carried out in the presence of a catalytically effective amount of a supported Group VIE metal containing hydrogenation catalyst at elevated temperatures and pressure and the mole ratio of amino compound to polyalkenyl ether glycol is less than 2:1 when zis greater than 1. SUMMARY OF THE INVENTION [0013] Severely sterically hindered secondary aminoether alcohols of the general formula 1 wherein R* and R2 are each independently selected from the group consisting of alkyl and hydroxyalkyl radicals having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms, or R* and R^ in combination with the carbon atom to which they are attached form a cycloalkyl group having 3 to 8 carbons; R^ is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbon atoms, and mixtures thereof, preferably 1 to 2 carbon atoms, preferably alkyl or hydroxyalkyl radicals having 1 to 4 carbon atoms, more preferably 1 to 2 carbon atoms; R4, R5, R6, R7, R8, R9, RlO^ ^d R! 1 are the same or different and are selected from hydrogen, alkyl or hydroxyalkyl radicals having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms, or cycloalkyl radicals having 3 to 8 carbons; R4, R5, R6, R7, R8, R9, R10, and R1 1 are preferably hydrogen provided that when R^ is hydrogen at least one of R4 and R5 bonded to the carbon which is directly bonded to the nitrogen atom is an alkyl or hydroxyalkyl radical, are prepared by a process involving reacting an organic carboxylic acid halide, an organic carboxylic acid anhydride or a ketene, or a mixture of any two or of all three thereof, of the formula 2: (Figure Removed wherein R12 and R13 are the same or different and each is selected from the group consisting of alkyl radicals having 1 to 4 carbon atoms, preferably 1 to 2 carbon atoms, most preferably methyl, or aryl radicals, preferably phenyl substituted with hydrogen, one or more alkyl radicals having 1-10 carbon atoms, preferably 1-4 carbon atoms, most preferably methyl in the para position, and mixtures thereof, and x is a halogen selected from the group consisting of F, Cl, Br, I and mixtures thereof, preferably Cl, and wherein Rx and RV are the same or different and are selected from the group consisting of hydrogen, alkyl radicals having 1-4 carbons, preferably 1 to 2 carbons, aryl radicals, preferably aryl radicals bearing substituents selected from the group consisting of hydrogen and one or more alkyl radicals having 1 to 10 carbons, preferably 1-4 carbons, and mixtures thereof, or Rx and Rv in combination with the carbon to which they are attached form a cycloalkyl radical having 3 to 8 carbons, preferably Rx and Ry are hydrogen or phenyl, with 50% sulfuric acid to fuming sulfuric acid, preferably 75% sulfuric acid to fuming sulfuric acid, more preferably 90% sulfuric acid to fuming sulfuric acid to produce monoacyl sulfate 3 and/or diacyl sulfate 4: (Figure Removed wherein R12/13 means that in the product the R group can be R12 or R13, or mixtures thereof, which are then reacted with a 1,4-dioxane of the formula 5: (Figure Removed wherein R4, R5, R6, R7, R8, R9, R10, and R11 are the same or different and are selected from hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbons, and mixtures thereof, preferably 1-2 carbons, and mixtures thereof, more preferably R4, R5, R6, R7, R8, R9, R10, and R11 are hydrogen, to yield material of the general formula 6 and/or 7: (Figure Removed or mixtures thereof. It is not necessary that the product from each reaction step be isolated before being reacted with the reactant of a subsequent reaction step up to this point. A cleavage product is produced. The mixing of the organic carboxylic acid halide, organic carboxylic acid anhydride, ketene or mixture thereof, with the sulfuric acid and the dioxane can be in any order or sequence. Thus, the anhydride, and halide, ketene or mixture thereof, can be mixed with the sulfuric acid and then mixed with the dioxane, or the dioxane can be first mixed with the sulfuric acid and then the anhydride, acid halide, ketene, or mixture thereof, can be added, or the anhydride, acid halide, ketene or mixture thereof can be mixed with the dioxane followed by the addition of the sulfuric acid. Thus, the combination of the anhydride, acid halide, ketene or mixture thereof with the dioxane and the sulfuric acid can be combined into a single reaction mixture and reacted as a mixture resulting in the one step production of the desired cleavage product. This cleavage product is then animated using an alkyl amine of the formula 8 (Figure Removed wherein Rl and R2 are the same of different and selected from the group consisting of alkyl and hydroxyalkyl radicals having 1 to 4 carbon atoms, and mixtures thereof, preferably 1 to 2 carbon atoms, more preferably methyl, or Rl and R^ in combination with the carbon atom to which they are attached form a cycloalkyl group having 3 to 8 carbons, and mixtures thereof; R is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbon atoms, and mixtures thereof, preferably 1 to 2 carbon atoms, preferably alkyl or hydroxyalkyl radicals having 1 to 4 carbon atoms, more preferably 1 to 2 carbon atoms, most preferably methyl, provided that when R^ is hydrogen then at least one of R4 and R^ is an alkyl or hydroxyalkyl radical, to yield material of the general formula 9: (Figure Removed [0014] The preferred compounds defined by the general formula 1 include: (Figure Removed 2-[2-( 1 -ethyl- 1 -methylpropylamino)ethoxy]ethanol. [0015] Typical starting materials are ketenes represented by the formula 2: wherein Rx and RY are the same or different and are selected from the group consisting of hydrogen, alkyl radicals having from 1 to 4 carbons, preferably 1 to 2 carbons, most preferably hydrogen, aryl radicals, preferably aryl radicals bearing substituents selected from the group consisting of hydrogen, one or more alkyl radicals having 1 to 10 carbons, preferably 1 to 4 carbons, and mixtures thereof, or Rx and Ry in combination with the carbon to which they are attached form a cycloalkyl radical having 3 to 8 carbons, and mixtures thereof, preferably Rx and RY are hydrogen or phenyl. [0016] The ketenes useful in the present invention can be prepared employing any of the processes typical in the art. Thus, for example, acetic acid can be subjected to high temperature dehydration in the presence of A1PO4, or acetone can be subjected to pyrolysis at from 500-750°C to yield ketene and methane. [0017] The ketene, organic carboxylic acid halide, organic carboxylic acid anhydride, or mixtures of any two or all three thereof, is reacted with 50% to fuming, preferably 75% to fuming, most preferably 90% to fuming sulfuric acid, H2SCO4, at preferably a 1 : 1 molar ratio to form the monoacyl sulfate 3 or in about a 2:1 molar ratio to form the diacyl sulfate 4. Excess sulfuric acid can be used at the practitioners discretion, but the use of excess acid would necessitate the practice of an additional separation step. The use of about a stoichiometric ratio, therefore, is preferred. The use of concentrated sulfuric acid (90% to fuming) is preferred. Fuming sulfuric acid I also known as oleum. It is a solution of sulfur trioxide in 100% sulfuric acid. 100% sulfuric acid is also referred to as monohydrate because it constitutes one molecule of SO3 combined with one molecule of HaO. The percent of free SO3 is used as a measure of oleum or fuming sulfuric acid strength. Thus, 20% fuming sulfuric acid constitutes 20% free SO3 over and above the 100% sulfuric acid carrier solvent. Twenty (20) % fuming sulfuric acid contains 20% SO3 and 80% H2SO4 (of 100% concentrated H2SO4) by weight. Oleum or fuming sulfuric acid can contain as high as 80%+ free SO3. Reaction can be conducted at about -80°C to about 150°C, preferably about -20°C to about 125°C at a pressure between about 1 bar to 100 bars, preferably about 1 bar to 50 bars, more preferably about 1 bar to 10 bars. The reaction can be carried out in an inert solvent such as sulfolane, hexanes, acetonitrile. Preferably the dioxane for the subsequent cleavage reaction is used as the solvent resulting hi a unified first step wherein the reaction mixture contains the carboxylic acid halide, the organic carboxylic acid anhydride, the ketene or mixture thereof, the sulfuric acid and the dioxane. This reaction mixture is then reacted under the condition subsequently described for the dioxane cleavage reaction. [0018] Acyl sulfate 3 or 4 is then reacted with a dioxane 5 which is typically of the formula: ,0 H3C O (Figure Removed Other substituted isomers can be readily envisioned. Preferably, the dioxane is Cleavage of the dioxane ring and reaction is for a time sufficient to achieve about 60-90% conversion to product. [0019] The reaction can be carried out either in the absence of solvent, in which case the dioxane serves as the solvent for the reaction, or in a solution containing an additional inert solvent such as acetonitrite or toluene, the reaction being conducted at temperatures of from about -80°C to about 200°C. [0020] Preferably, the dioxane serves as the solvent for the reaction. The molar ratio of dioxane to acyl sulfate, for the reaction of dioxane with acyl sulfate 3 is about 1:1 to about 10:1, preferably about 1:1 to about 8:1, most preferably about 1:1 to about 5:1, while the molar ratio of dioxane to acyl sulfate of formula 4 is about 2:1 to about 10:1, preferably about 2:1 to about 8:1, more preferably about 2:1 to about 5:1. Expressed differently, the dioxane to acyl sulfate ratio is about stoichiometric to about 10:1, preferably about stoichiometric to about 8:1, more preferably about stoichiometric to about 5:1. The temperature for the reaction of dioxane with acyl sulfate of general formula 3 is in the range of between about -80°C to about 200°C, preferably about -20°C to about 160°C, most preferably about -20°C to about 50°C, and the temperature for the reaction of dioxane with the acyl sulfate of general formula 4 is in the range of between about 50°C to about 200°C, preferably about 70°C to about 160°C, more preferably about 80°C to about 140°C. [0021] The ether cleavage process is described hi greater detail by Karger and Mazur hi "The Cleavage of Ethers by Mixed Sulfonic-Carboxylic Anhydrides", Journal of the American Chemical Society, 1968, 90, 3878-3879. See also, "Mixed sulfonic-carboxylic anhydrides. I. Synthesis and thermal stability. New syntheses of sulfonic anhydrides" Journal of Organic Chemistry, 1971,36,528; and "Mixed sulfonic-carboxylic anhydrides. II. Reactions with aliphatic ethers and amines" Journal of Organic Chemistry, 1971, 36,532. [0022] The reaction of a dioxane 5 with acyl sulfate 3 yields cleavage product of general formula 6, while the reaction of a dioxane 5 with diacyl sulfate 4 yields a cleavage product of the formula 7. [0023] The cleavage products 6 and 7 are then aminated using an amine 8, typically of the formulae: CH3 CH3 CH2CH3 CH2CH3 H3C-C-NH2, H3C-C-NH2, H3C-C-NH2 , H3C-C-NH2 CH3 H CH3 CH2CH3 preferably: CH3 I H3C-C-NH2 CH3 for a time sufficient to replace the sulfate group in cleavage products 6 and 7 with an amine 8. In the case of the animation of cleavage product 7, at least two moles of the amine 8 are required for each mole of 7. In general, the amine to cleavage product sulfonate group mole ratio is in the range of about stoichiometric to about 10:1, preferably about stoichiometric to about 8:1, more preferably about stoichiometric to about 4:1. In the case of the animation of either product 6 or product 7, the same aminated product 9 is produced: R1 R4 R6 R8 Rio o R* R2 - C- N - (L_(l_0_c_ i-o- C- C- Ry C- N - (_(_0_c_ 9a I H I I I I R3 R5 R? R9 Rll H R1 R4 R6 R8 R10 O 12/13 9b I3 H j? k7 t» fe" [0024] This amination step can be carried out under any conditions typical in the art. Amination can be conducted at atmosphere or at elevated pressure, elevated pressure being especially suitable when amination is to (Figure Removed be performed using relatively low boiling amines such at t-butylamine. [0025] Thus, amination can be conducted at pressures of from about atmospheric (1 bar) to about 100 bars, preferably about 1 to about 50 bars and at temperatures of from about 40°C to about 200°C, preferably about 40°C to about 125°C. The process can be performed under reflux but this is not absolutely necessary. An inert solvent optionally can be used such as benzene, toluene, diethyl ether, hexanes, and the like. [0026] This aminated product 9 is hydrolyzed to product 1 using a base, which is typically an alkali metal hydroxide, alkali metal carbonate, alkali metal alkoxide, such as sodium hydroxide, sodium carbonate, sodium methoxide, sodium tert-butoxide, etc. Reaction is conducted at about 20°C to about 110°C, preferably about 20°C to about 50°C. The process can be conducted under reflux. Solvents which can be used if either necessary or simply desirable include water and alcohols and mixtures thereof. The alcohol can be the same as that from which the alkoxide base is derived, i.e., methanol in the solvent for alkali metal methoxide. EXAMPLES [0027] The preparation of 2-(2-tert-buWlaminoethoxvtethanol (EETB). A 100 mL one-necked flask was charged with 1,4-dioxane (20 g, 0.23 mol, 20 mL) under a nitrogen atmosphere; acetic anhydride (4 mL, 4.28 g, 42 mmol) was added followed by the addition of 20% fuming sulfuric acid (1.04 mL, 2.0 g; contains 16.4 mmol of H2SO4) at room temperature. The reaction mixture was refluxed at 101 °C and checked by NMR. The *H NMR spectrum showed that products of cleavage reached a maximum after 18 h. The reaction mixture was evaporated under vacuum to dryness (bath 50°C, 15 mm of Hg). Toluene (50 mL) was added to the residue followed by the addition of terf-butylamine (30 mL, 21 g, 0.29 mol) at room temperature. The reaction mixture was gently (tertbutylamine BP = 44-46°C) refluxed for 30 h. Then, the reaction mixture was cooled to room temperature and filtered; the precipitate was washed with toluene. The filtrate was partially evaporated under vacuum to remove tertbutylamine. The residue was filtered and the precipitate was washed with toluene. The filtrate was evaporated under vacuum to give a yellow residual oil (4.5 g). The NMR spectra showed 2-(2-r-butylaminoethoxy)ethyl acetate of 60-70% purity. The character of signals in NMR spectrum suggests 2-(2- hydroxyethoxy)ethyl acetate as major impurity (signal of acetoxy group: singlet at 2.09 ppm, of etheral signals: m, 3.65-3.72 ppm, and ester signal: m, 4.21-4.27 ppm), as result of incomplete animation or hydrolysis during work up. [0028] The reflux of 2-(2-f-butylaminoethoxy)ethyl acetate (2 g, 10 mmol) with 15 mmol of NaOH in methanol (10 mL) for 6 h followed by evaporation under vacuum, extraction with diethyl ether and removing of solvent under vacuum gave 1.6 g of yellow oil, the NMR of which confirmed 2-(2-tertbutylaminoethoxy) ethanol (EETB) of 70-75% purity. The EETB is probably contaminated with diethylene glycol (extra protons in the range 3.59-3.73 ppm; by comparison with NMR data for diethylene glycol: 3.60 ppm, m, 4H; 3.74 ppm, m, 4H). [0029] The cleavage of 1.4-dioxane with diaetvl sulfate generated from fuming sulfuric acid and a twofold excess of acetic anhydride. The same reaction conditions were used as for the cleavage above using 20% fuming sulfuric acid and acetic anhydride (twofold excess: 1 equivalent for SO3, plus 2 equivalent for H2SO4, and plus 100% excess). Also, the animation with t- BuNH2 was carried out in an autoclave (bomb) to provide maximum completeness. [0030] A 100 mL one-necked flask was charged with 1,4-dioxane (30 g, 0.35 mol, 30 mL) under a nitrogen atmosphere; acetic anhydride (7.1 mL, 7.66 g, 75 mmol was added followed by the addition of 20% fuming sulfuric acid (1.04 mL, 2.0 g; contains 0.4 g, 5.0 mmol of SO3 and 1.6 g, 16.4 mmol of H2SO4) at room temperature. The reaction mixture was refluxed for 40 h and checked by NMR. The !H NMR spectrum showed the presence of products of cleavage. Reflux was continued for an additional 8 h. The NMR showed the same set of signals as after 40 h. The reaction mixture was evaporated under vacuum to dryness (the reaction mixture was protected from contact with moisture; the solvent was directly evaporated into a dry-ice trap using a dry membrane-type vacuum pump; bath 50°C, 5 mm of Hg). Toluene (50 mL) was added to the residue followed by the addition of terr-butylamine (30 mL, 21 g, 0.29 mol) at room temperature. The reaction mixture was stirred for 5 min and the reaction mixture was transferred into an autoclave (bomb) and stirred at approximately 170°C (175-180°C in the oil bath) for 13 h. The reaction mixture was cooled to room temperature and filtered from the precipitate. The precipitate was washed with toluene and the combined filtrate was evaporated in vacuum. Toluene was added to the residue and the mixture was washed with an aqueous solution of sodium carbonate. The organic layer was dried over magnesium sulfate and the solvent was evaporated in vacuum to give 3.4 g of yellow oil. The *H NMR analysis showed the desired 2-(2-t-butylaminoethoxy)ethylacetate product hi 70-75% purity. As in the previous reaction, the major byproduct is 2-(2- hydroxyethoxy)ethyl acetate; extra protons at 2.09 ppm (0.7 H, Ac), 3.58-3.72 (3H) and 4.20-4.24 (0.45 H, CH2OAc). Part of this product crystallized as colorless needles). [0031] Cleavage of 1.4-dioxane with diacetvl sulfate generated from fuming sulfuric acid and acetic anhydride (1 equivalent of acetic anhydride for SOi. plus 2 equivalent for H-SCM at 120°C. A 15 mL sealed tube was charged with 1,4-dioxane (10 g, 0.11 mol, 10 mL) and acetic anhydride (2.67 mL, 2.88 g, 28.2 mmol) was added followed by the addition of 20% fuming sulfuric acid (0.78 mL, 1.5 g; contains 0.3 g, 3.75 mmol of SO3 and 1.2 g, 12.23 mmol of H2SO4) at room temperature under a nitrogen atmosphere. The reaction mixture was stirred at 120-122°C for 24 hours and checked by NMR. The *H NMR spectrum showed presence of products of cleavage. The reaction mixture was evaporated under vacuum to dryness. Toluene (50 mL) was added to the residue followed by the addition of terr-butylamine (17 mL, 11.8 g, 0.16 mol) at room temperature. The reaction mixture was gently refluxed for 24 h, cooled to room temperature and filtered from the precipitate. The precipitate was washed with toluene and the combined filtrates were evaporated under vacuum. Toluene was added to the residue and the mixture was washed with an aqueous solution of sodium carbonate. The organic layer was dried over magnesium sulfate and the solvent was evaporated under vacuum to give 3.5 g of brown oil. The *H NMR analysis showed the desired product 2-(2-te/t-butylaminoethoxy)ethyl acetate of approximately 70% purity. The major by-products are 2-(2- hydroxyethoxy)ethyl acetate or 2-(2-acetoxyethoxy)ethyl acetate. [0032] Cleavage of 1.4-dioxane with diacetvl sulfate generated from sulfur trioxide and acetic anhydride. A 15 mL sealed tube was charged with dioxane (10 g, 0.115 mol), acetic anhydride (1.81 mL, 1.96 g, 19 mmol), and sulfur trioxide (1.54 g, 19 mmol) under a nitrogen atmosphere. The mixture was stirred at 119-123°C for 5 h (brown clear solution). The !H NMR analysis showed characteristic signals of cleavage products. The reaction mixture was concentrated under vacuum. The residue was stirred with tert-butyl amine (20 mL, 13.92 g, 0.19 mol) in toluene (30 mL) under gentle reflux for 24 h. The reaction mixture was cooled to room temperature, filtered, and the precipitate was washed with toluene. The filtrate was evaporated and the product was extracted with toluene. The extract was evaporated under vacuum to give 2 g of yellow - brown oil. The NMR test showed desired product 2-(2-tertbutylaminoethoxy) ethyl acetate of approximately 65% purity. We Claim: 1. A method for the synthesis of severely sterically hindered secondary aminoether alcohols of the formula (Formula Removed) wherein R1 and R2 are each selected from the group consisting of alkyl, hydroxylalkyl radicals having 1 to 4 carbon atoms or in combination with the carbon atom to which they are attached they form a cycloalkyl group having 3 to 8 carbon atoms, and R3 is selected from the group consisting of hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbon atoms, and mixtures thereof, and R4, R5, R6, R7, R8, R9, R10 and R11 are the same or different and are selected from the group consisting of hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbons provided that at least one of R4 or R5 bonded to the carbon atom directly bonded to the nitrogen atom is an alkyl or hydroxyalkyl radical when R3 is hydrogen, the process involving reacting an organic carahoxylic acid halide, an organic carboxylic acid anhydride, a ketene, or a mixture of any two or of all three thereof, of the formula (Formula Removed) wherein R12 and R13 are the same or different and are selected from the group consisting of alkyl radicals having 1 to 4 carbon atoms, aryl radicals bearing hydrogen or C1 to C10 alkyl radicals substituted thereon, and mixtures thereof, X is a halogen selected from the group consisting of F, CI, Br, I, and mixtures thereof, and Rx and Ry are the same or different and are selected from the group consisting of hydrogen, alkyl radicals having 1-4 carbons, aryl radicals, aryl radicals bearing substituents selected from the group consisting of hydrogen and one or more alkyi radicals having 1 to 10 carbons, and mixtures thereof, or Rx and Ry in combination with the carbon to which they are attached form a cycloalkyl radical having 3 to 8 carbons, with 50% sulfuric acid to fuming sulfuric acid to yield monoacylsulfatc (3) and/or diacylsulfate (4) of the formula (Formula Removed) which is then reacted with a dioxane of the formula (Formula Removed) wherein R4, R5, R6, R7, R8, R9, R10, and R11 are the same or different and are selected from hydrogen, alkyl and hydroxyalkyl radicals having 1 to 4 carbons to yield products of the structure 6 and/or 7: (Formula Removed) and mixtures thereof, which are then aminated with an alkyl amine of the formula (Formula Removed) wherein R1, R2 and R3 are as previously defined to yield material of the general formula 9 (Formula Removed) or mixtures thereof, which is then hydrolyzed with base to yield product (1). 2. The method as claimed in claim 1 for the synthesis of severely sterically hindered secondary aminoether alcohols using the organic carboxylic acid halide of the formula (Formula Removed) 3. The method as claimed in claim 1 for the synthesis of severely sterically hindered secondary aminoether alcohols using the organic caraboxylic acid anhydride of the formula (Formula Removed) 4. The method as claimed in claim 1 for the synthesis of severely sterically hindered secondary aminoether alcohols using a ketene of the formula (Formula Removed) 5. The method as claimed in any one of the preceding claims wherein R1 , R2 and R3 are methyl radicals. 6. The method as claimed in any one of the preceding claims wherein R4, R5, R6, R7, R8, R9, R10 and R11 are hydrogen, and Rx and RY are hydrogen or phenyl. 7. The method as claimed in any one of the preceding claims wherein the base is selected from alkali metal hydroxide, alkali metal alkoxide, or alkali metal carbonate. 8. The method as claimed in any one of the preceding claims wherein R1, R2, R3 are methyl, R4, R5, R6, R7, R8, R9, R10 and R11 are hydrogen and Rx and RY are hydrogen or phenyl. 9. The method as claimed in any one of the preceding claims wherein the ketene, organic carboxylic acid halide, organic carboxylic acid anhydride, mixture of any two or of all three thereof, and the H2SO4 are reacted in a stiochiometric ratio at a temperature between -80°C to 150°C, the resulting sulfate is reacted with the dioxane at a dioxane to sulfate ratio of stoichiometric to 10:1 to cleave the dioxane at a temperature between -80°C to 200°C, the resulting cleavage product is reacted with the alkyl amine in an amine to cleavage product mole ratio of stoichiometric to 10:1 at a pressure of from atmospheric (1 bar) to 100 bars, at a temperature of between 40°C to 200°C, and the aminated product is hydrolyzed with base at between 20°C to 110°C. 10. The method as claimed in any one of the preceding claims wherein the mixing of the ketene, organic carboxylic acid halide, organic carboxylic acid anhydride, mixture of any two or of all three, the sulfuric acid and the dioxane are combined in a single step, the reaction mixture being heated at a temperature of between -80°C to 200°C to produce a cleavage product, the cleavage product and the alkylamine are reacted at an amine to cleavage product ratio ranging from stoichiometric to 10:1 at a pressure from atmospheric (1 bar) to 100 bars at a temperature of between 40°C to 200°C, and the aminated product is hydrolyzed with base at between 20°C to 100°C.

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4328-DELNP-2006-GPA-(02-09-2011).pdf

4328-delnp-2006-gpa.pdf

4328-delnp-2006-pct-101.pdf

4328-delnp-2006-pct-105.pdf

4328-delnp-2006-pct-210.pdf

4328-delnp-2006-pct-220.pdf

4328-delnp-2006-pct-237.pdf

4328-delnp-2006-pct-304.pdf

4328-delnp-2006-pct-308.pdf

4328-delnp-2006-pct-311.pdf

4328-delnp-2006-pct-326.pdf

4328-delnp-2006-pct-373.pdf

4328-DELNP-2006-Petition-137-(02-09-2011).pdf