Preparation of Both Enantiomers of Ethyl 3-Hydroxybutanoate by Microbial Methods

Takeshi Sugai, Mitsuru Fujita, Kenji Mori

Research output: Contribution to journalArticlepeer-review

58 Citations (Scopus)


Both enantiomers of ethyl 3-hydroxybutanoate which are useful chiral starting materials for the synthesis of natural products containing CH3CH(OH)CH2R group have been prepared in a 3~18 g scale by microbial methods. Ethyl acetoacetate was enantio-selectively reduced to the 5-enantiomer by baker's yeast (in 83~90% e. e.) and by high temperature yeast (in 96% e. e., see Table 3). Asymmetric reductions by several brewer's yeasts (in 43~92% e. e.) and by commercially available HLADH, YADH (in 100% e. e.) gave also the 5-enantiomer. The R-enantiomer was prepared from poly (3-hydroxybutanoate) (PHB) produced by Zoogloea rami-gera, in 100% e. e. Their optical purities were determined by the HPLC analyses of the corresponding MTPA esters.

Original languageEnglish
Pages (from-to)1315-1321
Number of pages7
JournalNippon Kagaku Kaishi
Issue number9
Publication statusPublished - 1983
Externally publishedYes

ASJC Scopus subject areas

  • General Chemistry
  • General Chemical Engineering


Dive into the research topics of 'Preparation of Both Enantiomers of Ethyl 3-Hydroxybutanoate by Microbial Methods'. Together they form a unique fingerprint.

Cite this