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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355127Generated: October 30, 2026

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

https://huagongshe.com/reaction/355127

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 at reflux temperature for 24 hours. The resulting brown solid is filtered off, dissolved in 1 N NaOH, washed twice with water, 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 numberUS04377521
Source datasetuspto-grants-1983_03
ORD IDord-d99789d8bd1745d0b50601fa6bfd055e
Source noteuspto-grants-1983_03