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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613963Generated: October 25, 2026

1-Chloro-2-(trifluoromethyl)benzene → 2-(Trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1613963

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-(trifluoromethyl)benzeneHCID 6921—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178418416HCID 178418416—
CatalystPalladium ChlorideHCID 24290—
CatalystChiraphosHCID 3882352—
SolventWaterHCID 962—
Product2-(Trifluoromethyl)benzoic acidHCID 989991.5%

Reaction Conditions

Temperature240 °C

Reaction Steps

In an autoclave made of metal were placed 18 g of ortho-chlorobenzotrifluoride, 3.5 mg of palladium chloride, 170 mg of bisdiphenylphosphinobutane and 3.1 g of potassium carbonate. The air in the autoclave was replaced with carbon monoxide introduced thereinto in several times, after which carbon monoxide was further introduced to adjust its pressure therein to 30 kg/cm2. The reaction was carried out with stirring on a salt bath at a bath temperature of 240° C. After completion of the reaction, the reaction mixture was cooled to room temperature and water was added. The aqueous layer was separated and then acid was added thereto, followed by extraction from the aqueous layer. The ether layer was dried and then concentrated to obtain 3.9 g of ortho-trifluoromethylbenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194631
Source datasetuspto-grants-1993_03
ORD IDord-a96233ecf6c3490fac4a02b62c4ef30e
Source noteuspto-grants-1993_03