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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873621Generated: October 27, 2026

Oxalyl chloride → 3-(Chlorosulfonyl)-4-fluorobenzoyl chloride

https://huagongshe.com/reaction/873621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Chlorosulfonyl)-4-fluorobenzoic acidHCID 3929891—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-(Chlorosulfonyl)-4-fluorobenzoyl chlorideHCID 58107439—

Reaction Steps

To a suspension of 3-chlorosulfonyl-4-fluoro benzoic acid (2.5 g, 10 mmol) in methylene chloride at 0° C. is added oxalyl chloride (1.33 g, 11 mmol), followed by the addition of 1 drop of N,N,-dimethylformamide. The reaction mixture is warmed up to room temperature and stirred for an additional 4 h. The solvent is removed, and the residue is dried under vacuum for 1 hr to obtain the title compound as an oil, which is used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975439B2
Source datasetuspto-grants-2015_03
ORD IDord-104a5fa5897c4e989eb2bd193a57276c
Source noteuspto-grants-2015_03