Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621392Generated: October 26, 2026

2-Chloro-4-fluoro-5-nitrobenzyl cyanide → 2-(5-Amino-2-chloro-4-fluorophenyl)acetonitrile

https://huagongshe.com/reaction/621392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-fluoro-5-nitrobenzyl cyanideHCID 23036745—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product2-(5-Amino-2-chloro-4-fluorophenyl)acetonitrileHCID 23036747—

Reaction Steps

Hydrogen is injected at 25°-30° C., under normal pressure, into a mixture consisting of 8.9 g of 2-chloro-4-fluoro-5-nitrobenzyl cyanide, 1 g of Raney nickel in 90 ml of absolute ethanol, until the stoichiometric amount of hydrogen has been absorbed. After completion of the absorption of hydrogen, the reaction mixture is filtered and the alkaline filtrate is concentrated by evaporation. The residue consists of 7.5 g of 5-amino-2-chloro-4-fluorobenzyl cyanide having a melting point of 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824476
Source datasetuspto-grants-1989_04
ORD IDord-7608c611ec814e72aaa4b3184c2e28d3
Source noteuspto-grants-1989_04