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HRID 990873作成日:2026年10月26日

Water → (1R)-1-(2-(Trifluoromethyl)phenyl)ethylamine

https://huagongshe.com/reaction/990873

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ammonium HydroxideHCID 14923—
反応物Sodium borohydrideHCID 4311764—
反応物1-(2-trifluoromethyl-phenyl)-ethanone O-methyl-oximeHCID 54513608—
触媒Zirconium chloride (ZrCl4), (T-4)-HCID 9856075—
溶媒TetrahydrofuranHCID 8028—
生成物(1R)-1-(2-(Trifluoromethyl)phenyl)ethylamineHCID 278245017.1%

反応条件

温度25 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06462055B2
出典データセットuspto-grants-2002_10
ORD IDord-4b3bf6f75ef34627bf30faadf092c1bc
出典メモuspto-grants-2002_10