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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128165Generated: October 30, 2026

Ammonia → beta-Amino-2-chlorocinnamonitrile

https://huagongshe.com/reaction/128165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAcetonitrileHCID 6342—
Reactant2-ChlorobenzonitrileHCID 13391—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Productbeta-Amino-2-chlorocinnamonitrileHCID 70509051—

Reaction Steps

A 150 ml. portion of ammonia is condensed in a reaction flask and a small piece of sodium is added. The blue color is discharged by the addition of ferric chloride and 3.22 g. of sodium are added. After the color is discharged, 5.75 ml. of acetonitrile in 10 ml. of diethyl ether are added. The reaction is cooled in a dry ice-acetone bath and 13.3 g. of 2-chlorobenzonitrile in 25 ml. of tetrahydrofuran are added dropwise. The ammonia is allowed to evaporate, the solvent is blown off with nitrogen and water is added. The mixture is extracted with methylene chloride. The organic extracts are dried over sodium sulfate and filtered through Magnesol®. The filtrate is evaporated with the addition of hexanes giving β-amino-2-chlorocinnamonitrile as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259256
Source datasetuspto-grants-1981_03
ORD IDord-b7897ce0bbf346259502e5f1541ca2ad
Source noteuspto-grants-1981_03