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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352396Generated: October 25, 2026

Water → 4-(Benzyloxy)benzene-1-sulfonyl chloride

https://huagongshe.com/reaction/352396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzyl Phenyl EtherHCID 70352—
Solvent1,2-DichloroethaneHCID 11—
Product4-(Benzyloxy)benzene-1-sulfonyl chlorideHCID 4738385—

Reaction Steps

To a suspension of 22.4 g (146 mmol) of sulfur trioxide/DMF complex in 60 mL of anhydrous 1,2-dichloroethane at room temperature, was added a solution of 30 g (162 mmol) of benzylphenyl ether in 30 mL of anhydrous 1,2-dichloroethane. The resulting mixture was warmed to reflux and maintained there for 1 hour, cooled to room temperature and 10.8 mL (146 mmol) of thionyl chloride added. The reaction was then warmed to 75 C for 1 hour, cooled in an ice bath, 50 mL of water slowly added, then ethyl acetate. The layers were separated, washed with saturated sodium bicarbonate, brine, dried with magnesium sulfate, filtered and stripped. The resulting solids were triturated with hexane to afford 24.5 g of pure 4-(Benzyloxy)benzenesulfonyl chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06747027B1
Source datasetuspto-grants-2004_06
ORD IDord-be569f83d1ea421887b5ea785b7a15d0
Source noteuspto-grants-2004_06