Resolution of racemic mixtures of aliphatic acid esters

Claim 2

A process for enzymatically resolving racemic mixtures of partially water-soluble esters which are soluble to more than 25 millimolar in water at 25° C. comprising reducing the water solubility of a racemic mixture of said esters to less than 25 millimolar by means other than changing the chemical composition of the ester, contacting the racemic mixture of esters of reduced water solubility with a lipase enzyme from Candida cylindracea capable of stereospecifically resolving the racemic mixture by hydrolysis and stereospecifically resolving the racemic mixture.

Claim 3

A process for enzymatically resolving racemic mixtures of partially water-soluble esters which are soluble in water to more than 25 millimolar at 25° C. defined by the formula ##STR3## wherein R and R 1 represent hydrogen and C 1 -C 4 alkyl; R 2 represents C 1 -C 4 alkyl and X represents halogen, aliphatic or aromatic groups and substituted derivatives thereof with the proviso that the compounds are at least partially water soluble wherein R, R 1 and X are different comprising reducing the water solubility of a racemic mixture of said esters to below about 25 millimolar by means other than changing the chemical composition of the ester selected from the group consisting of (a) adding a salt to an aqueous solution of the lipase enzyme in which at least some of the ester is in solution in an amount sufficient to lower the solubility of the ester in the aqueous solution; and (b) a combination of (a) with a water immiscible organic solvent, contacting the racemic mixture of esters of reduced water solubility with a lipase enzyme from Candida cylindracea capable of stereospecifically resolving the racemic mixture by hydrolysis and stereospecifically resolving the racemic mixture.

Claim 4

A process for enzymatically resolving racemic mixtures of partially water-soluble esters which are soluble in water to more than 25 millimolar at 25° C. defined by the formula ##STR3## wherein R and R 1 represent hydrogen and C 1 -C 4 alkyl; R 2 represents C 1 -C 4 alkyl and X represents halogen, aliphatic or aromatic groups and substituted derivatives thereof with the proviso that the compounds are at least partially water soluble wherein R, R 1 and X are different comprising reducing the water solubility of a racemic mixture of said esters to below about 25 millimolar by means other than changing the chemical composition of the ester selected from the group consisting of (a) adding a salt to an aqueous solution of the lipase enzyme in which at least some of the ester is in solution in an amount sufficient to lower the solubility of the ester in the aqueous solution; and (b) a combination of (a) with a water immiscible organic solvent, contacting the racemic mixture of esters of reduced water solubility with a lipase enzyme from Candida cylindracea capable of stereospecifically resolving the racemic mixture by hydrolysis and stereospecifically resolving the racemic mixture.

Claim 5

The process as recited in claim 2 wherein R is C 1 -C 4 alkyl, R 1 is hydrogen, R 2 is C 1 -C 4 alkyl and X is halogen.

Claim 6

The process as recited in claim 2 wherein R is C 1 -C 2 alkyl and R 2 is C 1 -C 2 alkyl.

Claim 7

The process as recited in claim 2 wherein R is hydrogen, R 1 is methyl, and X is p-hydroxyphenyl.

Claim 8

The process as recited in claim 5 wherein R 2 is methyl.

Claim 9

The process as recited in claim 2 wherein R is hydrogen, R 1 is methyl and X is p-hydroxyphenoxy.

Claim 10

The process as recited in claim 7 wherein R 2 is methyl.

Claim 11

The process as recited in claim 3 wherein R and R 2 are each methyl.

Claim 12

The process as recited in claim 9 wherein X is chlorine.

Claim 13

The process as recited in claim 2 wherein X is a halogen of chlorine or bromine.

Claim 14

The process as recited in claim 2 wherein said solvent is selected from the group consisting of carbon tetrachloride, perchloroethylene and mixtures thereof.

Claim 15

The process as recited in claim 8 wherein said solvent is carbon tetrachloride.

Claim 16

The process as recited in in claim 2 wherein said salt is an at least partially water-soluble salt selected from the group consisting of alkali metal and alkaline earth metal halides, carbonates, bicarbonates, phosphates, sulfates, nitrates and mixtures thereof.

Claim 17

The process as recited in claim 14 wherein said salt is sodium chloride, sodium bicarbonate or mixtures thereof.

Claim 18

The process as recited in claim 2 wherein said esters are 2-chloropropionic acid esters.

Claim 19

The process as recited in claim 16 wherein said solvent is selected from the group consisting of carbon tetrachloride perchloroethylene and mixtures thereof.

Claim 20

The process as recited in claim 16 wherein said salt is sodium chloride, sodium bicarbonate or mixtures thereof.

Claim 21

The process as recited in claim 16 wherein the ester is methyl.

Claim 22

The process as recited in claim 16 wherein said racemate is resolved using said water insoluble solvent in combination with said insolubilizing salt.

Claim 23

The process as recited in claim 20 wherein the temperature of hydrolysis ranges from about 2° C. to about 8° C.