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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749482Generated: October 29, 2026

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

https://huagongshe.com/reaction/1749482

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrophenylacetonitrileHCID 12125—
ReactantAmmonia chlorideHCID 20976574—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product(3-Amino-phenyl)-acetonitrileHCID 484785096.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of (3-nitro-phenyl)-acetonitrile (2.00 g, 12.35 mmol), iron dust (2.07 g, 37.03 mmol) and ammonia chloride (1.96 g, 37.03 mmol) in EtOH (20 mL) and water (4 mL) was refluxed at 85° C. for 1 h. The reaction mixture was filtered through cellite and rinsed with EtOH. The combined filtrate was concentrated and the residue was purified by silica gel column chromatography (20% ethyl acetate in petroleum ether) to afford the title compound (1.57 g, 11.89 mmol, 96% yield) as a pale-yellow solid. MS (ESI) m/z 133.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156798B2
Source datasetuspto-grants-2015_10
ORD IDord-1d9bf41c61664ff0b9ff0ccb5dabf58e
Source noteuspto-grants-2015_10