反応式
[BH4-].[Na+].CO[N:5]=[C:6]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[C:14]([F:17])([F:16])[F:15])[CH3:7].O.[OH-].[NH4+]>O1CCCC1.[Cl-].[Cl-].[Cl-].[Cl-].[Zr+4]>[F:15][C:14]([F:16])([F:17])[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=1[CH:6]([NH2:5])[CH3:7]参加物
反応条件
- 温度
- 25 °C
実験手順
Sodium borohydride (1.17 g) is added slowly to a flask containing zirconium tetrachloride (1.8 g) in tetrahydrofuran (27 mL). A solution of 1-(2-trifluoromethyl-phenyl)-ethanone O-methyl-oxime (1.34 g) in tetrahydrofuran (7.7 mL) is added and the resulting solution is stirred at 25° C. for 12 hours. The reaction mixture is then cooled to 0° C. and water (16 mL) is slowly added. Excess ammonium hydroxide is added and the solution is extracted twice with ethyl acetate. The organic portion is washed twice with 1N hydrochloric acid. The aqueous (acid) layer is basified with sodium hydroxide and extracted twice with ethyl acetate. The organic layer is then washed with saturated aqueous sodium chloride and dried over anhydrous magnesium sulfate. The solvent is removed under reduced pressure to provide the desired product as a yellow oil (0.20 g).
後処理
- temperatureThe reaction mixture is then cooled to 0° C.
- extractionthe solution is extracted twice with ethyl acetate
- washThe organic portion is washed twice with 1N hydrochloric acid
- extractionextracted twice with ethyl acetate
- washThe organic layer is then washed with saturated aqueous sodium chloride
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent is removed under reduced pressure
出典と根拠
- ORDレコード
- ord-0d75a079af6a4b83b5f2ea444a3a513c
- 出典データセット
- uspto-grants-2001_07
- 特許番号
- US06255349B1
関連ノート
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