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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460310Generated: October 29, 2026

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

https://huagongshe.com/reaction/1460310

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 numberUS05070205
Source datasetuspto-grants-1991_12
ORD IDord-2756118b8d3f48728fd7d1f66c960af7
Source noteuspto-grants-1991_12