Benzo(B)Thiophene → 3-(5,6-Dimethoxybenzo[b]thien-2-yl)-3-oxo-propanoic acid methyl ester
反応式
[H-].[Na+].[C:3](=[O:8])([O:6][CH3:7])OC.[C:9]([C:12]1[S:16][C:15]2[CH:17]=[C:18]([O:23][CH3:24])[C:19]([O:21][CH3:22])=[CH:20][C:14]=2[CH:13]=1)(=[O:11])[CH3:10].S1C2C=CC=CC=2C=C1.[H-].[K+]>O1CCCC1.C(O)(=O)C>[CH3:7][O:6][C:3](=[O:8])[CH2:10][C:9]([C:12]1[S:16][C:15]2[CH:17]=[C:18]([O:23][CH3:24])[C:19]([O:21][CH3:22])=[CH:20][C:14]=2[CH:13]=1)=[O:11]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
A mixture of sodium hydride (60% dispersion in oil, 10.9 g) and dimethyl carbonate (18.7 ml) in dry tetrahydrofuran (210 ml) was stirred and heated at reflux under an atmosphere of nitrogen. A solution of 2-acetyl-5,6-dimethoxy-benzo[b]thiophene (21.0 g) in dry tetrahydrofuran (315 ml) was added dropwise over 30 min. Shortly after the addition of the benzothiophene solution had commenced potassium hydride (22.7% dispersion in oil) was added to initiate the reaction (sufficient to cause a permanent pink colour). When the evolution of gas had ceased (90 min.) the reaction mixture was cooled in an ice bath and treated with glacial acetic acid (34 ml). The resultant yellow solution was poured into ice-cold water (2 liter), stirred, and the yellow solid was filtered, washed with n-hexane and dried at 50° C. under vacuum to give 3-(5,6-dimethoxybenzo[b]thien-2-yl)-3-oxo-propanoic acid methyl ester (22.0 g). A portion crystallized from dichloromethane/diethyl ether had m.p. 129°-130° C.
後処理
- temperatureheated
- temperatureat reflux under an atmosphere of nitrogen
- additionwas added
- customthe reaction (sufficient
- custom(90 min.)
- temperaturewas cooled in an ice bath
- stirringstirred
- filtrationthe yellow solid was filtered
- washwashed with n-hexane
- customdried at 50° C. under vacuum
出典と根拠
- ORDレコード
- ord-c827f4d26d2b4429b74e7c675b94648f
- 出典データセット
- uspto-grants-1990_08
- 特許番号
- US04952571
反応ノート
読み込み中…