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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444281Generated: October 30, 2026

3-Nitrophenylacetonitrile → (3-Amino-phenyl)-acetonitrile

https://huagongshe.com/reaction/1444281

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrophenylacetonitrileHCID 12125—
CatalystIronHCID 23925—
Product(3-Amino-phenyl)-acetonitrileHCID 4847850—

Reaction Steps

A solution of 3-nitrophenyl acetonitrile (500 mg, 3.1 mmol) in 5% ACOH (10 ml) was heated to 80° C. Iron powder (1.5 g, 27 mmol) was then added and the resulting mixture stirred for 2 h. The reaction mixture was filtered through celite and the filter cake washed with MeCN (4×50 ml). The combined MeCN layers were evaporated in vacuo and the residue was re-dissolved in EtOAc (30 ml) followed by 2M HCl (30 ml). The aqueous layer was separated, basified to pH 10 with 6M NaOH, and extracted with EtOAc (3×80 ml). The combined organic layers were dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662839B2
Source datasetuspto-grants-2010_02
ORD IDord-cd28feba9d29476f811ddb95cd1e1540
Source noteuspto-grants-2010_02