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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274132Generated: October 30, 2026

2-Aminobenzonitrile → 2-[N-(5-methyl-2-nitrobenzylidene)amino]benzonitrile

https://huagongshe.com/reaction/274132

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzonitrileHCID 72913—
Reactant5-Methyl-2-nitrobenzaldehydeHCID 11805110—
SolventTolueneHCID 1140—
Product2-[N-(5-methyl-2-nitrobenzylidene)amino]benzonitrileHCID 2009452562.1%

Reaction Steps

Toluene (167 ml) and 2-aminobenzonitrile (19.7 g, 167 mmol) were added to 5-methyl-2-nitrobenzaldehyde (27.5 g, 167 mmol) as obtained in Reference Example 1, and the mixture was stirred and refluxed for 14 hours, followed by cooling. The resultant crystals were filtered off, washed with a mixed solvent of hexane/toluene (2:1, 150 ml) and hexane (150 ml) twice to give 27.5 g of 2-[N-(5-methyl-2-nitrobenzylidene)amino]benzonitrile. In addition, the solid precipitated from the filtrate was filtered off and washed with hexane (100 ml and 50 ml) to give 10.0 g of the compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387684
Source datasetuspto-grants-1995_02
ORD IDord-9274c858a04045b6946923ef4ef2faa2
Source noteuspto-grants-1995_02