반응식
[SH:1][CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)=[O:4].[C:11](=[O:14])([O-])[O-].[K+].[K+].CO[C:19]1[CH:24]=[CH:23][C:22]([CH:25]2[O:27][CH:26]2[C:28]([NH2:30])=[O:29])=[CH:21][CH:20]=1>C(#N)C>[OH:27][CH:26]([CH:25]([S:1][CH2:2][C:3](=[O:4])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[C:22]1[CH:23]=[CH:24][CH:19]=[CH:20][C:21]=1[C:5]1[CH:10]=[CH:9][C:8]([O:14][CH3:11])=[CH:7][CH:6]=1)[C:28]([NH2:30])=[O:29]참가 물질
5
실험 절차
To a solution of 8.0 g (0.052 mol) of 2-mercapto-1-phenylethanone in 120 mL of acetonitrile was added 0.3 g (0.052 mol) of powdered potassium carbonate and 10.1 g (0.052 mol) of 3-(4-methoxyphenyl)oxiranecarboxamide. After the mixture was stirred and heated at reflux under nitrogen for 3.5 hours the solvent was removed under reduced pressure. The crude product was chromatographed on silica gel (150 g). The column was eluted with ethyl acetate, fractions 7-13 containing the product were combined and the solvent was removed under reduced pressure. The residue was crystallized from ethyl acetate to give 4.0 g (22%) of rac.-(R,*R*)-α-hydroxy-4-methoxyphenyl- β-[(2-oxo-2 -phenylethyl)thio]benzenepropanamide, mp 132°-134°.
후처리
- temperatureheated
- temperatureat reflux under nitrogen for 3.5 hours the solvent
- customwas removed under reduced pressure
- customThe crude product was chromatographed on silica gel (150 g)
- washThe column was eluted with ethyl acetate, fractions 7-13 containing the product
- customthe solvent was removed under reduced pressure
- customThe residue was crystallized from ethyl acetate
출처 및 근거
- ORD 기록
- ord-ca016424f88d4acdba6b9945f017e20a
- 출처 데이터셋
- uspto-grants-1991_02
- 특허 번호
- US04992432
연결된 노트
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