Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892759Generated: October 26, 2026

Ethanol → N-(4-cyanophenyl)-4-amino-3-nitropyridine

https://huagongshe.com/reaction/892759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-AminobenzonitrileHCID 13396—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
ProductN-(4-cyanophenyl)-4-amino-3-nitropyridineHCID 19791284—

Reaction Steps

According to the method of J.C.S. Perkin Trans. I, 1979, 135, p-cyanoaniline (6.894 g, 58.4 mmol) was added to a solution of 4-chloro-3-nitropyridine (9.26 g, 58.4 mmol) in ethanol (200 ml) and the mixture was stirred at room temperature for 18 hours. The resulting yellow suspension was poured into 500 ml of ice-cold dilute ammonia and filtered. The solid was treated with 150 ml of boiling ethanol, cooled in ice, and filtered to give N-(4-cyanophenyl)-4-amino-3-nitropyridine, 12.15 g, as a bright yellow powder, m.p. 210°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120747
Source datasetuspto-grants-1992_06
ORD IDord-311d6e67ac3c48c49b38f8bacf7171dc
Source noteuspto-grants-1992_06