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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202176Generated: October 30, 2026

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

https://huagongshe.com/reaction/2202176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodiumHCID 5360545—
Reactant4-(Benzyloxy)benzenesulfonic acidHCID 11335143—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(Benzyloxy)benzene-1-sulfonyl chlorideHCID 473838589%

Reaction Steps

A solution of 55 ml (639 mmol) of oxalyl chloride in 250 ml of dichloromethane is added dropwise to a solution of 61 g (213 mmol) of the sodium salt of 4-benzyloxybenzenesulfonic acid in 200 ml of dimethylformamide, while maintaining the temperature between −20° C. and −10° C. After addition, the reaction medium is slowly brought back to ambient temperature and then stirred for 18 h, poured onto ice and extracted with ethyl acetate. The organic phase is washed with water and with a saturated aqueous solution of sodium chloride and concentrated under vacuum. 54 g (89%) of 4-benzyloxybenzenesulfonyl chloride are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-89771a2e8b2f45d48704390c98b4b636
Source noteuspto-grants-2016_06