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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384871Generated: October 27, 2026

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

https://huagongshe.com/reaction/384871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-Chloro-3-FluorobenzaldehydeHCID 2724985—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
Product2-Amino-2-(4-chloro-3-fluorophenyl)acetonitrileHCID 61650338—

Reaction Steps

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)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367838B2
Source datasetuspto-grants-2013_02
ORD IDord-c58137df8a8b447993670e0bde63c0ca
Source noteuspto-grants-2013_02