Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450402Generated: October 30, 2026

4'-Nitro-[1,1'-biphenyl]-2-carbonitrile → 2-(4-Aminophenyl)benzonitrile

https://huagongshe.com/reaction/1450402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-Nitro-[1,1'-biphenyl]-2-carbonitrileHCID 12714795—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product2-(4-Aminophenyl)benzonitrileHCID 1393926—

Reaction Steps

6.0 g (26.8 mmol) of 2'-cyano-4-nitrobiphenyl (prepared according to B. Sain, J. S. Sandhu, J. Org. Chem. 1990, 55, 2545) were dissolved in a mixture of 60 ml ethanol and 60 ml ethyl acetate, and the solution was filled into an autoclave. After addition of 660 mg 10% Pd on charcoal the mixture was set under an atmosphere of hydrogen (2-3 bar). The reduction was carried out at room temperature, the course of the reaction monitored by thin layer chromatography, and it had completed after 2.5 h. The catalyst was filtered and the solvent distilled off in vacuo. The title amine was obtained by crystallization from hexane as a white powder,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602136
Source datasetuspto-grants-1997_02
ORD IDord-617a7a949a2f4932820fd26f561ae1f5
Source noteuspto-grants-1997_02