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HRID 384871作成日:2026年10月26日

Ammonia → 2-Amino-2-(4-chloro-3-fluorophenyl)acetonitrile

https://huagongshe.com/reaction/384871

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物WaterHCID 962—
反応物Trimethylsilyl cyanideHCID 82115—
反応物4-Chloro-3-FluorobenzaldehydeHCID 2724985—
触媒Titanium isopropoxideHCID 11026—
溶媒MethanolHCID 887—
生成物2-Amino-2-(4-chloro-3-fluorophenyl)acetonitrileHCID 61650338—

反応手順

To a solution of 25.0 g (158 mmol) 4-chloro-3-fluorobenzaldehyde in 130 ml methanol and 175 ml methanol saturated with ammonia were added 54.9 ml (52.7 g, 185 mmol) tetraisopropyl orthotitanate and the mixture stirred at ambient temperature for 1.5 hours. Then 20.35 ml (16.14 g, 163 mmol) trimethylsilyl cyanide were added drop-wise and the resulting mixture stirred at ambient temperature for further 2 hours. The reaction mixture was poured onto 1500 ml iced water and extracted with ethyl acetate. The combined organic phases were washed with brine, dried over Na2SO4 and evaporated. The crude product was purified by flash-chromatography on silica gel with a gradient of heptane and 0 to 50% ethyl acetate. rac-Amino-(4-chloro-3-fluoro-phenyl)-acetonitrile was obtained as orange oil: MS (ISN): 183.2 (M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367838B2
出典データセットuspto-grants-2013_02
ORD IDord-c58137df8a8b447993670e0bde63c0ca
出典メモuspto-grants-2013_02