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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70558Generated: October 29, 2026

p-Bromobenzenesulfonyl chloride → 4-bromo-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/70558

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant2-(Methylamino)ethanolHCID 8016—
SolventChloroformHCID 6212—
Product4-bromo-N-(2-hydroxyethyl)-N-methylbenzenesulfonamideHCID 39403192—

Reaction Steps

A solution of 4-bromobenzenesulfonyl chloride (1.10 g) in chloroform (10 mL) was stirred in an ice bath, during which N-methylethanolamine (5 mL) was slowly added dropwise thereto. The mixture was returned to room temperature and stirred for about 2.5 hours. The reaction solution was quenched with concentrated hydrochloric acid with stirring again in an ice bath. The mixed solution was poured into 6 M hydrochloric acid (10 mL) as such, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure to give a crude product of 4-bromo-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide as a colorless oil (1.339 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-72b90cee6b8d4917905f3a688a617b53
Source noteuspto-grants-2014_09