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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233268Generated: October 31, 2026

2-Chloro-4-nitrobenzoic acid → HCID 966782, compound

https://huagongshe.com/reaction/2233268

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-nitrobenzoic acidHCID 7448—
Reactant2-AminobenzonitrileHCID 72913—
SolventThionyl ChlorideHCID 24386—
ProductHCID 966782HCID 96678229.1%

Reaction Steps

A solution of 2-chloro-4-nitrobenzoic acid (6.00 g, 29.8 mmol) in thionyl chloride (20 ml) was heated at reflux for 2.5 hours. The reaction was cooled, the excess thionyl chloride was evaporated in vacuo and the residue was azeotroped with toluene (2×25 ml). The residue was taken up in toluene (35 ml), 2-aminobenzonitrile (1.75 g, 14.8 mmol) was added and the reaction heated at reflux for 2 hours. The reaction was cooled, the solvent was removed in vacuo and the residue was absorbed onto silica gel. Purification by flash chromatography on silica gel, eluting with dichloromethane, yielded N-(2-cyanophenyl)-2-chloro-4-nitrobenzamide (1.30 g, 27% yield) as a pale yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709479B1
Source datasetuspto-grants-2010_05
ORD IDord-0e6b7a69e7d347fc8c33f18ca82d5180
Source noteuspto-grants-2010_05