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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730593Generated: October 30, 2026

2-Fluorobenzoic acid → 2-Fluoro-5-chlorosulfonylbenzoic acid

https://huagongshe.com/reaction/1730593

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluorobenzoic acidHCID 9935—
ReactantChlorosulfonic acidHCID 24638—
Product2-Fluoro-5-chlorosulfonylbenzoic acidHCID 608984—

Reaction Steps

o-Fluorobenzoic acid is reacted with chlorosulfonic acid by the method of Example 1 to form 2-fluoro-5-chlorosulfonylbenzoic acid. This is reacted with 3,5-dimethylpiperidine by the method of Example 1 to form 2-fluoro-5-(3,5-dimethylpiperidinosulfonyl)benzoic acid. This product (0.0015 mole) is heated to 60° C. with diethylamine (10 ml.) and ethanol (3.0 ml.) to form a clear solution, and the reaction mixture is then heated aat reflux temperature for 24 hours. The resulting brown solidis filtered off, dissolved in 1N NaOH, washed twice with ether, and the product precipitated by the addition of concentrated HCl. Recrystallization from diethyl ether replaced by isopropyl ether yields the product, m.p. 139.5-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03992441
Source datasetuspto-grants-1976_11
ORD IDord-051de76c3825486dae1de1726384e39c
Source noteuspto-grants-1976_11