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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107676Generated: October 31, 2026

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

https://huagongshe.com/reaction/2107676

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 numberUS04935430
Source datasetuspto-grants-1990_06
ORD IDord-6cdfadb3b6f8494aa7d9eff6d5f02195
Source noteuspto-grants-1990_06