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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503083Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → N-(4-Chlorophenyl)-4-methoxybenzenesulfonamide

https://huagongshe.com/reaction/1503083

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
Reactant4-ChloroanilineHCID 7812—
ReactantTriethylamineHCID 8471—
SolventDichloromethaneHCID 6344—
ProductN-(4-Chlorophenyl)-4-methoxybenzenesulfonamideHCID 59867169%

Reaction Steps

To a solution of 4-methoxybenzenesulfonyl chloride (5.0 g, 24 mmol) and 4-chloroaniline (3.1 g, 24 mmol) in dichloromethane (24 mL) at 0° C. was added triethylamine (3.4 mL, 24 mmol) over 10 minutes. The ice bath was removed, and the mixture was stirred for 16 hr. The mixture was diluted with dichloromethane (100 mL) and the combined solution was washed with water (50 mL) and brine (50 mL). The organic solution was dried over MgSO4, filtered, and evaporated, and the crude product was purified by silica gel chromatography (15-60% EtOAc/Hex). Product-containing fractions were pooled, evaporated, and dried under high vacuum to yield 4.9 g (69%) of the product as a tan-colored oil: 1H-NMR (CDC3) δ 10.17 (s, 1H), 7.71 (d, 2H), 7.61 (d, 2H), 7.04 (d, 2H), 6.96 (d, 2H), 2.19 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212134B2
Source datasetuspto-grants-2015_12
ORD IDord-1f054c19907c40dfabb53d9c7b519679
Source noteuspto-grants-2015_12