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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886181Generated: November 2, 2026

4-Aminobenzonitrile → 4-(4-Cyanophenyl)amino-2,6-dimethyl-3-nitropyridine

https://huagongshe.com/reaction/1886181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobenzonitrileHCID 13396—
Reactant4-Chloro-2,6-dimethyl-3-nitropyridineHCID 10702725—
SolventEthanolHCID 702—
Product4-(4-Cyanophenyl)amino-2,6-dimethyl-3-nitropyridineHCID 10611943—

Reaction Steps

A solution of 4-chloro-2,6-dimethyl-3-nitropyridine (9.80 g, 52.5 mmol) and 4-aminobenzonitrile (6.20 g, 52.5 mmol) in ethanol (160 ml) was stirred at room temperature for 16 hours. The solvent was removed under reduced pressure and the residue was dissolved in dichloromethane (200 ml), and washed with saturated aqueous sodium bicarbonate (100 ml). The organic phase was dried (MgSO4) and concentrated under reduced pressure to give a gum which was crystallised by adding ether (100 ml) and sonicating for 5 minutes. The yellow solid (9.80 g, 70%) was filtered off and dried in vacuo, mp 171°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05149814
Source datasetuspto-grants-1992_09
ORD IDord-e4dc61f694c74e4dab5c172d61c72a9d
Source noteuspto-grants-1992_09