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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287714Generated: November 1, 2026

Aniline → 4-Anilino-3-nitro-5-phenylsulphamyl-benzoic acid

https://huagongshe.com/reaction/1287714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant4-Chloro-5-chlorosulfonyl-3-nitrobenzoic acidHCID 89892—
SolventEthyl AcetateHCID 8857—
Product4-Anilino-3-nitro-5-phenylsulphamyl-benzoic acidHCID 21506088—

Reaction Steps

To a solution of 4-chloro-3-nitro-5-chlorosulphonyl-benzoic acid (6 g) in ethyl acetate (50 ml), aniline (7.5 g) was added, while stirring. The reaction mixture was stirred for a further 8 hours and filtered. The filtrate was evaporated, and the residue was dissolved in a mixture of aqueous sodium hydrogen carbonate and diethyl ether. The aqueous layer was separated, and the 4-anilino-3-nitro-5-phenylsulphamyl-benzoic acid was precipitated by addition of 4N hydrochloric acid. After recrystallization from aqueous ethanol (25% ethanol in water), the melting point was 249°-250° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-677d8dc495e74f239dd4a4a67036a709
Source noteuspto-grants-1976_10