反応式
[CH3:1][C:2]1([CH3:11])[CH:4]([CH:5]=[O:6])[CH:3]1[C:7]([O:9][CH3:10])=[O:8].[Cl:12][C:13](Cl)([Cl:18])[C:14]([F:17])([F:16])[F:15].[Cl-].[NH4+]>CN(C)C=O.[Zn]>[CH3:1][C:2]1([CH3:11])[CH:4]([CH:5]([OH:6])[C:13]([Cl:18])([Cl:12])[C:14]([F:17])([F:16])[F:15])[CH:3]1[C:7]([O:9][CH3:10])=[O:8]参加物
反応条件
- 温度
- 0 °C
実験手順
To a solution of 156 mg (1.00 mmol) of methyl 2,2-dimethyl-3-formylcyclopropane carboxylate and 0.226 ml (2.00 mmol) of 1,1,1-trichlorotrifluoroethane in 1 ml of dimethylformamide (DMF), 98 mg (1.50 mmol) of zinc powder was added at 0° C., and the mixture was stirred at 0° C. for 20 minutes, and at 50° C. for 7 hours. Then, 1 ml of a saturated ammonium chloride aqueous solution was added, and the mixture was extracted with diethyl ether (2 ml×5 times). The extract was dried over anhydrous magnesium sulfate, then filtered and concentrated under reduced pressure. The product was purified by thin layer chromatography (silica gel, dichloromethane/hexane=1/2) to obtain 232 mg of methyl 2,2-dimethyl-3-(1-hydroxy-2,2-dichloro-3,3,3-trifluoropropyl)cyclopropanecarboxylate (a mixture of two stereoisomers in a ratio of 55:45) as a colorless oil.
後処理
- waitat 50° C. for 7 hours
- extractionthe mixture was extracted with diethyl ether (2 ml×5 times)
- dry with materialThe extract was dried over anhydrous magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe product was purified by thin layer chromatography (silica gel, dichloromethane/hexane=1/2)
出典と根拠
- ORDレコード
- ord-4cdf7f52003241a1aa6684d971e6fa31
- 出典データセット
- uspto-grants-1989_09
- 特許番号
- US04864052
関連ノート
読み込み中…