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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6355Generated: October 23, 2026

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

https://huagongshe.com/en/reaction/6355

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 numberUS05248681
Source datasetuspto-grants-1993_09
ORD IDord-2bc83680343e4dc3bafc2ceb0ba1db4f
Source noteuspto-grants-1993_09