Hydrochloric Acid → 3-Hydroxy-2-(p-methoxyphenyl)-5-trifluoromethylbenzo[b]thiophene
반응식
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:26]=[CH:25][C:8]([CH2:9][S:10][C:11]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][C:12]=2[C:13]([O:15]C)=O)=[CH:7][CH:6]=1.O.Cl>CN(C)C=O>[OH:15][C:13]1[C:12]2[CH:17]=[C:18]([C:21]([F:22])([F:24])[F:23])[CH:19]=[CH:20][C:11]=2[S:10][C:9]=1[C:8]1[CH:25]=[CH:26][C:5]([O:4][CH3:3])=[CH:6][CH:7]=1참가 물질
반응 조건
- 온도
- 75 °C
실험 절차
To a mixture of sodium hydride (50% dispersion in mineral oil) (134 mg, 2.79 mmol) in N,N-dimethylformamide (3 ml) at 75° C. under a nitrogen atmosphere was added dropwise with stirring a solution of methyl 2-(p-methoxybenzylthio)-5-trifluoromethylbenzoate (500 mg, 1.40 mmol) in N,N-dimethylformamide (10 ml). After stirring 30 minutes at 75° C., the mixture was poured into water (50 ml), the mixture brought to pH5 with 2N hydrochloric acid, the product extracted with diethyl ether, the combined extracts washed with water, dried (sodium sulfate), and evaporated. The residue was chromatographed on a column of silica gel (Merck 7734, packed as a slurry in 25:1 hexane-ether). Elution with 25:1 hexane-ether containing 1% acetic acid afforded the desired product as a white solid upon evaporation of the appropriate fractions; yield 385 mg (85%); m/z 324 (M+.).
후처리
- additionwas added dropwise
- extractionthe product extracted with diethyl ether
- washthe combined extracts washed with water
- dry with materialdried (sodium sulfate)
- customevaporated
- customThe residue was chromatographed on a column of silica gel (Merck 7734
- washElution with 25:1 hexane-ether containing 1% acetic acid
출처 및 근거
- ORD 기록
- ord-3feef361eedd4a3a9a00a5a6d88a2783
- 출처 데이터셋
- uspto-grants-1987_05
- 특허 번호
- US04663344
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