Imidazole → (S)-Benzyl 3-[tert-butyldimethylsilyloxy]glutaramate
반응식
[CH2:1]([O:8][C:9](=[O:17])[CH2:10][C@@H:11]([OH:16])[CH2:12][C:13]([NH2:15])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N1C=CN=C1.[Si:23](Cl)([C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:25])[CH3:24]>CN(C)C=O>[CH2:1]([O:8][C:9](=[O:17])[CH2:10][C@@H:11]([O:16][Si:23]([C:26]([CH3:29])([CH3:28])[CH3:27])([CH3:25])[CH3:24])[CH2:12][C:13]([NH2:15])=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1참가 물질
실험 절차
(S)-Benzyl-3-hydroxyglutaramate (49.5 g) was dissolved in anhydrous dimethylformamide (50 ml) and added to a 500 ml flask containing solid imidazole (17.1 g). To this a solution of tert-butyldimethylsilyl chloride (34 g) in dimethylformamide (120 ml) was added and reaction flask was cooled in an ice-bath. The reaction was quenched by addition of water-saturated ethyl acetate. The mixture was stirred at ambient temperature. To this water was added and the biphasic mixture was stirred for 1 hour. The mixture was then washed with water. The organic phases were mixed and washed with water to remove traces of dimethylformamide. The organic phase was evaporated under reduced pressure to yield (S)-benzyl-3-(tert-butyl dimethylsilyloxy)glutaramate.
후처리
- additionadded to a 500 ml flask
- customreaction flask
- temperaturewas cooled in an ice-bath
- customThe reaction was quenched by addition of water-saturated ethyl acetate
- additionTo this water was added
- stirringthe biphasic mixture was stirred for 1 hour
- washThe mixture was then washed with water
- additionThe organic phases were mixed
- washwashed with water
- customto remove traces of dimethylformamide
- customThe organic phase was evaporated under reduced pressure
출처 및 근거
- ORD 기록
- ord-9ef076b2aecd4c04aa2d50babc6c418a
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09273333B2
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