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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249363Generated: November 3, 2026

Ammonium Chloride → alpha-(4-Amino-2-chlorophenyl)-4-chloro-alpha-methylbenzeneacetonitrile

https://huagongshe.com/reaction/1249363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Chloro-alpha-(2-chloro-4-nitrophenyl)-alpha-methylbenzeneacetonitrileHCID 13770355—
CatalystIronHCID 23925—
SolventTolueneHCID 1140—
Productalpha-(4-Amino-2-chlorophenyl)-4-chloro-alpha-methylbenzeneacetonitrileHCID 13770357—

Reaction Steps

A mixture of 20 parts of 4-chloro-α-(2-chloro-4-nitrophenyl)-α-methylbenzeneacetonitrile, 7 parts of iron powder, 250 parts of ammonium chloride solution 0.78N and 200 parts of methylbenzene was stirred and refluxed for 3 hours. The reaction mixture was filtered hot. The aqueous phase was separated and washed with methylbenzene. The combined organic layers were washed successively with water, sodium hydrogen carbonate solution and again with water, dried and evaporated. The residue was washed with 1,1'-oxybisethane and dried, yielding 10 parts of α-(4-amino-2-chlorophenyl)-4-chloro-α-methylbenzeneacetonitrile; mp. 135.2° C. (intermediate 24).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631278
Source datasetuspto-grants-1986_12
ORD IDord-213fe6b655e64d3aadd2ac6e91d16df5
Source noteuspto-grants-1986_12