(-)-3-t-Butyldimethylsilyloxybutyric acid phenylthioester → (-)-3-Hydroxybutyric acid phenylthioester

HRID 1090329노트

반응식

HRID 1090329 반응식
[C:1]1([S:7][O:8][C:9](=[O:21])[CH2:10][CH:11]([O:13][Si](C(C)(C)C)(C)C)[CH3:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1>C(O)(=O)C.C1COCC1.O>[C:1]1([S:7][O:8][C:9](=[O:21])[CH2:10][CH:11]([OH:13])[CH3:12])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

참가 물질

3

반응물 1

HCID 54408146(-)-3-t-Butyldimethylsilyloxybutyric acid phenylthioester

생성물 1

HCID 53886232(-)-3-Hydroxybutyric acid phenylthioester수율 94%

시약·촉매·용매 1

HCID 21877175AcOH THF water용매

반응 조건

온도
50 °C

실험 절차

To 3.26 g (10.4 mmol) of (-)-3-t-butyldimethylsilyloxybutyric acid phenylthio ester was added 50 ml of acetic acid: THF:water (3:1:1) and the mixture was stirred at 50° C. for 24 hours. The resultant was concentrated and distilled (128° to 130° C./0.8 mmHg) to give 1.91 g of (-)-3-hydroxybutyric acid phenylthio ester (yield: 94%).

후처리

  1. concentrationThe resultant was concentrated
  2. distillationdistilled (128° to 130° C./0.8 mmHg)

출처 및 근거

ORD 기록
ord-1ad6a6c7ae2049f7b6f8f5e35693f85f
출처 데이터셋
uspto-grants-1992_01
특허 번호
US05081238

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