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Ethyl benzoylformate → (-)-Ethyl mandelate

HRID 2166210
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HRID 2166210 반응식
[BH4-].[Na+].C(O)(=O)[C@@H]([C@H](C(O)=O)O)O.[C:13]1([C:19](=[O:25])[C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C1COCC1>[OH:25][C@H:19]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:20]([O:22][CH2:23][CH3:24])=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 15349Ethyl benzoylformateHCID 444305L-Tartaric acidHCID 4311764Sodium borohydride

생성물 1

HCID 6951556(-)-Ethyl mandelate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

반응 조건

온도
70 °C

실험 절차

To a dispersion of 0.43 g (11.3 mmol) of sodium borohydride in THF (35 ml), there was added 1.70 g (11.3 mmol) of L-(+)-tartaric acid, and the mixture was heated under reflux for four hours in an oil bath at 70° C. with stirring. The resulting mixture was cooled in a cryostat at -20° C., a solution of 0.5 g (2.8 mmol) of ethyl phenylglyoxylate in THF (5 ml) was added dropwise over a period of ten minutes, and stirring was continued for 19 hours. The reaction mixture was treated in the same manner as in Example 6, giving 0.44 of ethyl (R)-(-)-2-hydroxy-2-phenylacetate, having a specific rotation [α]D16 of -109° (cl. 00, CHCl3).

후처리

  1. temperaturethe mixture was heated
  2. temperatureThe resulting mixture was cooled in a cryostat at -20° C.
  3. stirringstirring
  4. additionThe reaction mixture was treated in the same manner as in Example 6

출처 및 근거

ORD 기록
ord-23d7742559c24a7d8cf6c67f17defabd
출처 데이터셋
uspto-grants-1990_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04943652

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