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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384871생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/384871

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물WaterHCID 962—
반응물Trimethylsilyl cyanideHCID 82115—
반응물4-Chloro-3-FluorobenzaldehydeHCID 2724985—
촉매Titanium isopropoxideHCID 11026—
용매MethanolHCID 887—
생성물2-Amino-2-(4-chloro-3-fluorophenyl)acetonitrileHCID 61650338—

반응 단계

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)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367838B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-c58137df8a8b447993670e0bde63c0ca
출처 메모uspto-grants-2013_02