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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763756Generated: October 31, 2026

4-Chlorobenzenesulfonyl chloride → Benzenesulfonamide, 4-chloro-N-(2-hydroxyethyl)-N-methyl-

https://huagongshe.com/reaction/1763756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
Reactant2-(Methylamino)ethanolHCID 8016—
SolventTetrahydrofuranHCID 8028—
ProductBenzenesulfonamide, 4-chloro-N-(2-hydroxyethyl)-N-methyl-HCID 108691—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 20 parts of tetrahydrofuran is added 3.9 parts of N-methyl-ethanolamine. To this solution, 10 parts of tetrahydrofuran containing 5 parts of p-chlorobenzenesulfonyl chloride is added with stirring. After completion of the addition, the resultant mixture is stirred as it is for a while, and then heated for about 1 hour on a water bath at 50° C. to terminate the reaction. Then, the salt is removed by filtration, and the filtrate is freed from the solvent, whereby an oily substance is obtained. This oily substance is subjected to distillation under reduced pressure to obtain 4.2 parts of a distillate, b.p. 180° C./0.5 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113463
Source datasetuspto-grants-1978_09
ORD IDord-5f6c9c12dad547abb9366f118ec830bb
Source noteuspto-grants-1978_09