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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860962Generated: October 31, 2026

Water → 2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoic acid

https://huagongshe.com/reaction/1860962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantTrifluoromethanesulfonic acidHCID 62406—
Reactant2-(3,5-Bis(trifluoromethyl)phenyl)propan-2-olHCID 620779—
ReactantHCID 178418416HCID 178418416—
SolventDichloromethaneHCID 6344—
Product2-(3,5-Bis(trifluoromethyl)phenyl)-2-methylpropanoic acidHCID 9835948—

Reaction Steps

A 185 ml stainless steel autoclave was charged under argon with 25 ml of dichloromethane, 22.30 ml (0.25 mol) of trifluoromethane sulfonic acid and 0.45 ml (25 mmol) of water. The autoclave was sealed and pressurized with 30 bar of carbon monoxide. Then under stirring a solution of 14.13 g (50 mmol) of 2-(3,5-bis-trifluoromethyl-phenyl)-propan-2-ol in 35 ml of dichloromethane was added with a pump within 50 min at 20° C. and the reaction mixture was stirred for additional 2 h. Thereafter the autoclave was vented and the biphasic reaction mixture was treated in an ice bath with a solution of 13.2 g of sodium hydroxide in 130 ml of water. The organic phase was removed and the aqueous phase was washed with dichloromethane. After filtration, 35 ml of 36.5% hydrochloric acid solution were added to the aqueous phase under stirring at 8-12° C. The resulting suspension was extracted twice with dicloromethane and, after drying with sodium sulfate, the organic phase was evaporated and the solid residue dried at room temperature and 10 mbar vacuum. 14.98 g of 2-(3,5-bis-trifluoromethylphenyl)-2-methyl-propionic acid were isolated as light brown crystals with m.p. 105.5-107° C. and 99.0% purity according to HPLC analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531597B2
Source datasetuspto-grants-2003_03
ORD IDord-04c0bf0f189e49acb8dc9b6d020df6ea
Source noteuspto-grants-2003_03