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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602607Generated: October 29, 2026

Ammonia → 3-Amino-2-methylbenzonitrile

https://huagongshe.com/reaction/1602607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxygenHCID 977—
Reactant3-Chloro-2-methylanilineHCID 6894—
ReactantHCID 178418546HCID 178418546—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Amino-2-methylbenzonitrileHCID 25484289%

Reaction Conditions

Temperature225 °C

Reaction Steps

283 g (2.0 mol) of 3-chloro-2-methylaniline are dissolved in 250 ml of N-methylpyrrolidone and admixed with 200 g (2.23 mol) of CuCN. The reaction mixture is subsequently stirred under N2 and at 225° C. for six hours. After cooling to 100° C., the reaction mixture is poured into 2.5 l of 25 percent ammonia solution and stirred at 25° C. for one hour. During this time, the atmospheric oxygen oxidizes the Cu(I) nitrile complex of the product to a water-soluble Cu(II) salt, which is evident by the formation of the intensively blue tetramine complex. Some of the CuCl remains undissolved as a white solid and can be easily removed by filtration with suction. The filtrate is extracted with approximately 2 l of methyl tert-butyl ether and then washed with ammonia water and finally three times with water. The organic phase is dried over sodium sulfate and concentrated, affording 255 g (89% yield of crude product) of a dark oil which can be purified by recrystallization from cyclohexane/toluene (5:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981758
Source datasetuspto-grants-1999_11
ORD IDord-cb031e2eee66493f9bac9edadda20ecd
Source noteuspto-grants-1999_11