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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036891Generated: November 3, 2026

2-Nitrobenzaldehyde → 4-[(2-Nitrophenyl)methylideneamino]benzonitrile

https://huagongshe.com/reaction/1036891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitrobenzaldehydeHCID 11101—
Reactant4-AminobenzonitrileHCID 13396—
SolventEthanolHCID 702—
Product4-[(2-Nitrophenyl)methylideneamino]benzonitrileHCID 61646379.3%

Reaction Steps

The mixture of 4-aminobenzonitrile (20 g, 0.17 mol) and 2-nitrobenzaldehyde (28.2 g, 0.17 mol) in anhydrous ethanol was heated to reflux for 3 h. The reaction mixture was cooled to room temperature. The solvent was removed under reduced pressure. The residue was washed with diethyl ether to give 4-(2-nitrobenzylideneamino)benzonitrile as yellow solid (33.7 g, yield 79.3%) LC/MS m/e obsd. (ESI+) [(M+H)+] 252.10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-4e7a7291dd9c4b8c98ba6eb171ccb03d
Source noteuspto-grants-2013_10