Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472122Generated: October 30, 2026

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

https://huagongshe.com/reaction/472122

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 numberUS08633196B2
Source datasetuspto-grants-2014_01
ORD IDord-8d3113bdf07143b2ae41a7945afe61ca
Source noteuspto-grants-2014_01