Method for the production of (r)- and (S)-8-chloro-6-hydroxyoctanic acid alkyl esters by enzymatic reduction
View Patent ↗The invention relates to a method for the production of (R)- or (S)-8-chloro-6-hydroxyoctanoic acid alkyl esters of the general formula (R)-II or (S)-II in which R has the meaning C 1-4 -alkyl, from 8-chloro-6-oxooctanoic acid alkyl esters of the general formula I in which R has the above meaning, by enzymatic reduction using alcohol dehydrogenases, such as Lactobacillus brevis or Thermoanaerobium brokii , in the presence of cofactor regeneration systems. The resulting (R)- and (S)-8-chloro-6-hydroxyoctanoic acid esters can be converted in a known manner into (R)-α-lipoic acid and (S)-α-lipoic acid, respectively.
1. A method for the production of (R)-S-chloro-6-hydroxyoctanoic acid alkyl esters of the formula (R)-II,
in which R has in each case the meaning C 1-4 -alkyl, characterized in that 8-chloro-6 -oxooctanoic acid alkyl esters of the formula I are reduced enzymatically using alcohol dehydrogenases or carbonyl reductases in the presence of NAD(H) or NADP(H) as cofactor.
2. A method for the production of (S)-8-chloro-6-hydroxyoctanoic acid alkyl esters of the formula (S)-II,
in which R has in each case the meaning C 1-4 -alkyl, characterized in that 8-chloro-6-oxooctanoic acid alkyl esters of the formula I are reduced enzymatically using alcohol dehydrogenases or carbonyl reductases in the presence of NAD(H) NADP(H) as cofactor.
3. The method as claimed in claim 1 , characterized in that an alcohol dehydrogenase from Thermoanaerobium brokii is employed.
4. The method as claimed in claim 2 , characterized in that an alcohol dehydrogenase from Lactobacillus brevis is employed.
5. The method as claimed in according to one of claims 1 – 4 , characterized in that a cofactor regeneration system which shifts the reduction equilibrium is included in the enzymatic reduction.