Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263925Generated: October 26, 2026

Chlorosulfonic acid → 4-Chloro-5-chlorosulfonyl-2-ethoxybenzoic acid

https://huagongshe.com/reaction/2263925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant4-Chloro-2-ethoxybenzoic acidHCID 18954604—
SolventDichloromethaneHCID 6344—
Product4-Chloro-5-chlorosulfonyl-2-ethoxybenzoic acidHCID 86612877—

Reaction Conditions

Temperature5 °C

Reaction Steps

4-Chloro-2-ethoxybenzoic acid (9.4 g, 47 mmol) was added in several portions to cold chlorosulfonic acid (55 mL, Aldrich) stirring at 0-10° C., and the resulting solution was heated at ˜60° C. for 2 h. The resulting dark solution was poured into ice (800 g), and then 500 mL of dichloromethane was added. After stirring for 15 min, the layers were separated and the aqueous layer was extracted with 200 mL of dichloromethane. The organic layers were washed in turn with brine, combined, dried over magnesium sulfate, filtered, and concentrated at room temperature. Crystallization from ether/hexane gave 3.4 g of 4-chloro-5-chlorosulfonyl-2-ethoxybenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851626B2
Source datasetuspto-grants-2010_12
ORD IDord-97f5c11b03684e6b9c6e1bf8ef197155
Source noteuspto-grants-2010_12