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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399477Generated: October 27, 2026

Benzenesulfonyl chloride → 2'-Chloro-4'-nitrobenzenesulfonanilide

https://huagongshe.com/reaction/399477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant2-Chloro-4-nitroanilineHCID 8492—
SolventPyridineHCID 1049—
Product2'-Chloro-4'-nitrobenzenesulfonanilideHCID 231836—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-4-nitroaniline (4.33 g), benzenesulphonyl chloride (3.25 ml) and pyridine (2.5 ml) was stirred and heated to 100° C. for 18 hours. The mixture was cooled to ambient temperature and partitioned between methylene chloride and 2M aqueous hydrochloric acid. The organic phase was washed with water, dried and evaporated. The residue was recrystallised from ethyl acetate to give N-(2-chloro-4-nitrophenyl)benzenesulphonamide (6.07 g), m.p. 155°-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821246
Source datasetuspto-grants-1998_10
ORD IDord-c466971758344711aafc5413143c01f3
Source noteuspto-grants-1998_10