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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413040Generated: October 26, 2026

Chloroacetyl chloride → 2-Chloro-N-(4-chlorobenzenesulfonyl)acetamide

https://huagongshe.com/reaction/2413040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant4-ChlorobenzenesulfonamideHCID 66824—
Product2-Chloro-N-(4-chlorobenzenesulfonyl)acetamideHCID 676503—

Reaction Steps

The reactant N-chloroacetyl 4-chlorobenzene sulfonamide was prepared by mixing 30.0 g of 4-chlorobenzene sulfonamide and 60.0 ml of chloroacetylchloride. The mixture was refluxed for 6 hours, allowed to cool, and stand at room temperature overnight. The crystalline product was removed by filtration, washed repeatedly with hexane, and dried. The product consisted of 32.5 g of reactant (m.p. 122°-124° C.). Structure was confirmed by IR and NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495365
Source datasetuspto-grants-1985_01
ORD IDord-6ff650ebc91f4cc8b8beabbdb27ea031
Source noteuspto-grants-1985_01