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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1356686Generated: October 25, 2026

Water → 2-chloro-N-methoxybenzenesulfonamide

https://huagongshe.com/reaction/1356686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Chlorobenzenesulfonyl chlorideHCID 76187—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
SolventPyridineHCID 1049—
Product2-chloro-N-methoxybenzenesulfonamideHCID 1850931964%

Reaction Steps

Methoxylamine hydrochloride (0.95 g (11.4 mmol)) was suspended in pyridine (4.0 ml). To this, under cooling with ice and with stirring, 2-chlorobenzenesulfonyl chloride (2.11 g (10.0 mmol)) was added and the mixture was stirred under cooling with ice for one hour and at room temperature for one hour. Water (50.0 ml) was added to the reaction mixture and the resulting mixture was extracted with ethyl acetate. The extract was washed with water, dilute hydrochloric acid and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give 1.41 g (64%) of 2-chloro-N-methoxybenzenesulfonamide as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586617B1
Source datasetuspto-grants-2003_07
ORD IDord-a4efb0fd2c384e50846b9f1491dd9f57
Source noteuspto-grants-2003_07