Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1036960Generated: November 2, 2026

3-Nitrobenzaldehyde → HCID 178510045, compound

https://huagongshe.com/reaction/1036960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-NitrobenzaldehydeHCID 7449—
Reactant4-AminobenzonitrileHCID 13396—
SolventTolueneHCID 1140—
ProductHCID 178510045HCID 178510045—

Reaction Steps

A mixture of 4-amino-benzonitrile (23.6 g, 0.2 mmol) in toluene (200 mL) was treated with a solution of 3-nitro-benzaldehyde (30.2 g, 0.2 mmol) in toluene (50 mL). The resultant mixture was allowed to reflux for 6 h. Toluene was removed under vacuum. The residue was purified by recrystallization from ethanol to afford 4-{[1-(3-nitro-phenyl)-meth-(E)-ylidene]-amino}-benzonitrile as yellow solid (50 g, yield %: 95.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546427B2
Source datasetuspto-grants-2013_10
ORD IDord-738c0bda75304e0b9d41e1954a0f9ee5
Source noteuspto-grants-2013_10