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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47847Generated: October 27, 2026

Ammonia → 2-Amino-4-chloro-5-methylbenzonitrile

https://huagongshe.com/reaction/47847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-Bromo-5-chloro-4-methylanilineHCID 3334656—
ReactantHCID 178418546HCID 178418546—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product2-Amino-4-chloro-5-methylbenzonitrileHCID 1085586566.4%

Reaction Steps

To a solution of 2-bromo-5-chloro-4-methylaniline (13.0 g 58.96 mmol) in N-methylpyrrolidinone (100 ml) was added copper(I) cyanide (10.56 g, 118 mmol). The reaction mixture was placed in an oil bath preheated to 163° C. and stirred at this temperature for 2 h. The reaction mixture was allowed to cool to room temperature and then poured in ice-water (300 ml) and aqueous ammonia (90 ml). The brown precipitate was collected by filtration, washed with water (150 ml), dissolved in dichloromethane and the insoluble material was removed by filtration. The filtrate was washed with brine (100 ml), dried (MgSO4) and concentrated in vacuo. Purification, on gradient elution with dichloromethane in petroleum ether 60-80° C. (65 to 95%), afforded a white solid (6.52 g), mp 180° C.; 1H-NMR (DMSO-d6) 2.14 (s, 3H, 4-CH3), 6.11 (s, 2H, NH2), 6.86 (s, 1H, 6-H), 7.39 (s, 1H, 3-H); MS (FAB, m/z) 166,168 [(M+H)+; 90%, 40% respectively; Cl isotopic pattern]; FAB-HRMS: measured 166.0307; calculated for C8H8ClN2 (M+H)+ 166.0298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699861B1
Source datasetuspto-grants-2004_03
ORD IDord-fd14e7fc615443658bae30f67ef9eeae
Source noteuspto-grants-2004_03