Acetaldehyde → (1S)-1-Methylthiocarbonyloxyethyl-2-methylpropanoate

HRID 558063노트

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HRID 558063 반응식
[O-]Cl.[Na+].CS.C(=O)C.[CH3:9][CH:10]([CH3:22])[C:11]([O:13][CH:14]([O:18][C:19]([CH3:21])=[S:20])[CH:15](C)C)=[O:12]>P([O-])([O-])([O-])=O>[CH3:21][C:19]([O:18][C@H:14]([O:13][C:11](=[O:12])[CH:10]([CH3:22])[CH3:9])[CH3:15])=[S:20]

참가 물질

6

실험 절차

A 20-L, multi-necked, cylindrical reactor, fitted with a mechanical stirrer, a nitrogen inlet and an outlet connected to an oxidation bath, and a bleach bath (14% NaOCl) to oxidize librated methanethiol and acetaldehyde is charged with racemic 2-methyl-1-methylthiocarbonyloxypropyl 2-methylpropanoate (2b) (5.32 kg, 25.8 mol) and 0.8 M phosphate buffer (10 L, pH 7.0). Solid supported Candida antarctica lipase A (125 g, NOVOZYME® 735, NOVOZYME®; CHIRAZYME™ L-5, Roche Diagnostics; or other suppliers) is slowly added while stirred. The reaction mixture is stirred at room temperature (22-24° C.) for ca. 18 hours.

후처리

  1. customconnected to an oxidation bath, and a bleach bath
  2. additionis slowly added
  3. stirringThe reaction mixture is stirred at room temperature (22-24° C.) for ca. 18 hours

출처 및 근거

ORD 기록
ord-3525701c7a124f948883bc250d388855
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08062870B2

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