Water → 4-Methoxy-2-methoxycarbonyl-3-(2-phenylethyl)benzo[b]thiophene
反応式
[SH:1][C:2]1[CH:17]=[CH:16][CH:15]=[C:14]([O:18][CH3:19])[C:3]=1[C:4](=O)[CH:5]=[CH:6][CH:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH2:8]1.C(N(CC)CC)C.Br[CH2:28][C:29]([O:31][CH3:32])=[O:30].O>ClCCl>[CH3:19][O:18][C:14]1[C:3]2[C:4]([CH2:5][CH2:6][C:7]3[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=3)=[C:28]([C:29]([O:31][CH3:32])=[O:30])[S:1][C:2]=2[CH:17]=[CH:16][CH:15]=1参加物
実験手順
To a solution of 2′-mercapto-6′-methoxydihydrochalcone (1.2 g) and triethylamine (0.92 mL) in dichloromethane (10 mL) was added methyl bromoacetate (0.46 mL), and the mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was dissolved in methanol (15 mL). To the solution was added sodium methoxide (28% methanol solution, 1.7 mL), and the mixture was stirred at room temperature overnight. The crystals precipitated from the reaction mixture were collected by filtration and dried under reduced pressure to give the title compound (1.09 g).
後処理
- extractionthe resulting mixture was extracted with diethyl ether
- washThe extract was washed with water and brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was removed under reduced pressure
- dissolutionthe residue was dissolved in methanol (15 mL)
- additionTo the solution was added sodium methoxide (28% methanol solution, 1.7 mL)
- stirringthe mixture was stirred at room temperature overnight
- customThe crystals precipitated from the reaction mixture
- filtrationwere collected by filtration
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-201aafc2a161429aa9fc849cac73612d
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07566699B2
反応ノート
読み込み中…