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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088662Generated: November 3, 2026

4-Aminobenzonitrile → 4-[N-(4-Cyanophenyl)amino]-3-nitropyridine

https://huagongshe.com/reaction/1088662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzonitrileHCID 13396—
Reactant4-Chloro-3-nitropyridineHCID 2735781—
SolventEthanolHCID 702—
Product4-[N-(4-Cyanophenyl)amino]-3-nitropyridineHCID 1056200686.6%

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 the title compound as a bright yellow powder, (12.15 g), m.p. 210°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963560
Source datasetuspto-grants-1990_10
ORD IDord-64cd5925305940b99730126fac585964
Source noteuspto-grants-1990_10