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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873838Generated: October 26, 2026

Potassium Hydroxide → 2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoic acid

https://huagongshe.com/reaction/1873838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium methanesulfinateHCID 2733271—
Reactant2-Bromo-4-(trifluoromethoxy)benzoic acidHCID 59447444—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
Product2-(Methylsulfonyl)-4-(trifluoromethoxy)benzoic acidHCID 59447309—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a 16 ml vial was loaded 2-bromo-4-(trifluoromethoxy)benzoic acid (225 mg, 0.79 mmol), sodium methylsulfinate (161 mg, 1.58 mmol), CuI (301 mg, 1.58 mmol), KOH (44 mg, 0.79 mmol, in 0.1 ml water) and 4 ml dimethyl sulfoxide. The reaction mixture was flushed with nitrogen, sealed and heated at 120° C. for 5 hours. After cooling to room temperature, it was diluted with 40 ml ether/ethyl acetate (1:1), 30 ml brine and 10 ml 3N HCl. The mixture was filtered through a pad of celite. The layers were separated, and the organic portion was dried over sodium sulfate, filtered and concentrated. The residue was purified with HPLC on a reverse phase column eluted with water and acetonitrile gradient solvent to give desire product as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304434B2
Source datasetuspto-grants-2012_11
ORD IDord-e7aea2d81efd422eabbdaf4b78451d50
Source noteuspto-grants-2012_11