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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956456Generated: November 2, 2026

Benzenesulfonyl chloride → Benzenesulfonamide, N-(4-nitrophenyl)-

https://huagongshe.com/reaction/1956456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant4-NitroanilineHCID 7475—
SolventPyridineHCID 1049—
ProductBenzenesulfonamide, N-(4-nitrophenyl)-HCID 231837—

Reaction Steps

A solution of 4-nitroaniline (4-7) (13.8 g, 100 mmol) and phenylsulfonyl chloride (14 mL, 100 mmol) in pyridine (50 mL) was heated at 100° C. for 2 h. The resultant solution was concentrated, and the residue dissolved in ethyl acetate. The organic extract was washed successively with 2M hydrochloric acid, sat. aq. sodium bicarbonate brine, dried over magnesium sulfate, filtered and concentrated under vacuum. The residue was dissolved in a minimum amount of ethyl acetate with warning, and hexane added until the solution turned cloudy. The mixture was allowed to cool slowly to RT and then chilled at 0° C. The yellow solid precipitated was obtained by filtration. Further drying under vacuum overnight provide N-phenylsulfonyl-4-nitroaniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780480
Source datasetuspto-grants-1998_07
ORD IDord-515796fdc4424f8c8a84136218437d66
Source noteuspto-grants-1998_07