Water → (4-Methoxyphenyl)[5-[(phenylmethyl)thio]-2-thienyl]methanone
反応式
[CH2:1]([SH:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].Br[C:12]1[S:13][C:14]([C:17](=[O:26])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[CH:15][CH:16]=1.O>CN(C=O)C>[CH2:1]([S:8][C:12]1[S:13][C:14]([C:17](=[O:26])[C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[CH:15][CH:16]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
6
反応条件
- 温度
- 25 °C
実験手順
Benzyl mercaptan (1.24 g, 0.01 mol) was added to a stirred mixture of sodium hydride (50% oil dispersion, 0.44 g, 0.11 mol) and degassed DMF (10 mL). The resulting mixture was warmed cautiously until gas evolution ceased. After cooling to 25° C., a solution of 2-bromo-5-(4-methoxybenzoyl)thiophene (2.97 g, 0.01 mol) in DMF (10 mL) was added dropwise. After complete addition, the mixture was heated on the steam bath for 2.5 hours and poured into waTER (200 mL). The aqueous mixture was extracted with ether (2×200 mL) and the extracts were washed with water, saturated NaCl solution and dried (Na2SO4). After evaporation of the solvent, the residue was collected with the aid of hexane and dried, 1.98 g, m.p. 103°-105° C.
後処理
- customdegassed DMF (10 mL)
- temperatureThe resulting mixture was warmed cautiously until gas evolution
- additionAfter complete addition
- temperaturethe mixture was heated on the steam bath for 2.5 hours
- extractionThe aqueous mixture was extracted with ether (2×200 mL)
- washthe extracts were washed with water, saturated NaCl solution
- dry with materialdried (Na2SO4)
- customAfter evaporation of the solvent
- customthe residue was collected with the aid of hexane
- customdried
出典と根拠
- ORDレコード
- ord-f1d6fc5116004de9b68c5f6380bbb4e5
- 出典データセット
- uspto-grants-1984_12
- 特許番号
- US04486444
反応ノート
読み込み中…