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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40790Generated: October 25, 2026

Water → N-benzhydryl-4-(bromomethyl)benzenesulfonamide

https://huagongshe.com/reaction/40790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzhydrylamineHCID 7036—
ReactantTriethylamineHCID 8471—
Reactant4-(Bromomethyl)benzenesulfonyl chlorideHCID 2734409—
SolventDichloromethaneHCID 6344—
ProductN-benzhydryl-4-(bromomethyl)benzenesulfonamideHCID 67021864—

Reaction Steps

Benzhydrylamine (640 μL) was dissolved in dichloromethane (5.0 mL). To the solution, triethylamine (645 μl) and 4-(bromomethyl)benzenesulfonyl chloride (1.0 g) were added at 0° C., and the mixture was stirred at room temperature for 2 hours. To the reaction mixture, water (10 mL) was added, and the resultant mixture was then extracted with chloroform (30 mL). The organic layer was washed with brine (15 mL), dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (40% ethyl acetate/hexane) to obtain the title compound (753 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530490B2
Source datasetuspto-grants-2013_09
ORD IDord-39757e3b8a604a86b768458e01915af5
Source noteuspto-grants-2013_09