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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892770Generated: October 27, 2026

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

https://huagongshe.com/reaction/892770

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 numberUS05120747
Source datasetuspto-grants-1992_06
ORD IDord-975684f4a4d3454c813050aacdfc93c0
Source noteuspto-grants-1992_06