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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356704Generated: October 26, 2026

Water → 4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilide

https://huagongshe.com/reaction/1356704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
ReactantBenzenamine, 4-chloro-N-ethyl-2-nitro-HCID 97006—
SolventTetrahydrofuranHCID 8028—
Product4'-Chloro-4-cyano-N-ethyl-2'-nitrobenzenesulfonanilideHCID 1850926564.6%

Reaction Steps

To a suspension of sodium hydride (60%, 0.10 g (2.50 mmol)) in tetrahydrofuran (THF)(3.0 ml), 4-chloro-N-ethyl-2-nitroaniline (0.40 g (1.99 mmol)) was added with stirring at room temperature. To the mixture, after stirring for 30 minutes at room temperature, 4-cyanobenzenesulfonyl chloride (0.50 g (2.48 mmol)) was added and the resulting mixture was stirred at room temperature for 3 hours. The reaction mixture was poured into water and the resulting mixture was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography with ethyl acetate-hexane (1:2) as eluent, to give 0.47 g (64%) of the title compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586617B1
Source datasetuspto-grants-2003_07
ORD IDord-ee92ba0fa7e3409690faf65a571f39f1
Source noteuspto-grants-2003_07