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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934713Generated: October 28, 2026

Acetone → 2-Fluoro-5-methanesulfonyl-benzoic acid

https://huagongshe.com/reaction/1934713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantSodium SulfiteHCID 24437—
Reactant2-Fluoro-5-chlorosulfonylbenzoic acidHCID 608984—
SolventWaterHCID 962—
SolventSodium CarbonateHCID 10340—
Product2-Fluoro-5-methanesulfonyl-benzoic acidHCID 22467566—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of sodium sulphite (10.6 g) in water (20 mL) was warmed to 80° C. and slowly added with stirring to a solution of 5-chlorosulfonyl-2-fluorobenzoic acid (10 g) in acetone (10 mL), saturated aqueous sodium carbonate being added simultaneously for keeping the liquid in alkaline. The mixture was stirred at 60° C. for one and a half hours, and concentrated in vacuo. The residue was suspended in a mixture of ethanol (20 mL) and water (20 mL), then iodomethane (2.61 mL) was added to the mixture. The reaction mixture was stirred for 2 hours at 60° C. and for an hour at 100° C. After cooling to ambient temperature, ethanol was removed in vacuo. The resultant aqueous solution was acidified with concentrated hydrochloric acid. The aqueous solution was extracted with chloroform (3 times), and the combined organic layer was dried over magnesium sulfate. After evaporation of the solvent, the residual oil was crystallized from ethanol to give 2-fluoro-5-methanesulfonylbenzoic acid (563.6 mg) as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384080B1
Source datasetuspto-grants-2002_05
ORD IDord-04f9da3fbed9413784c8fbd1a775d643
Source noteuspto-grants-2002_05