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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992065Generated: October 31, 2026

4-Chlorobenzoic Acid → 4-Chloro-3-(chlorosulphonyl)benzoic acid

https://huagongshe.com/reaction/1992065

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoic AcidHCID 6318—
ReactantChlorosulfonic acidHCID 24638—
Product4-Chloro-3-(chlorosulphonyl)benzoic acidHCID 75613—

Reaction Steps

At 5-10° C., to stirred chlorosulfonic acid (200 mL) was added 4-chlorobenzoic acid (78 g, 0.5 mol). The reaction mixture was then brought up to 150˜160° C. for 5 hours. After being cooled down to room temperature, the reaction mixture was slowly poured onto a large amount of ice and extracted with ether. The combined organic extracts were washed with ice water and dried over anhydrous magnesium sulfate. Evaporation of solvents afforded 4-chloro-3-(chlorosulfonyl)benzoic acid as a solid (76 g), which was directly used in the next steps.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645771B2
Source datasetuspto-grants-2010_01
ORD IDord-0ecbc521b4944894ae27a9f0f030af3a
Source noteuspto-grants-2010_01