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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613964Generated: October 25, 2026

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

https://huagongshe.com/reaction/1613964

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-(trifluoromethyl)benzeneHCID 6921—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 178418416HCID 178418416—
CatalystPalladium ChlorideHCID 24290—
CatalystChiraphosHCID 3882352—
SolventWaterHCID 962—
Product2-(Trifluoromethyl)benzoic acidHCID 989914.8%

Reaction Conditions

Temperature210 °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 23 g of sodium 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 for 5 hours on a salt bath at a bath temperature of 210° 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 with ether. The ether layer was dried and then concentrated to obtain 2.8 g of ortho-trifluoromethylbenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194631
Source datasetuspto-grants-1993_03
ORD IDord-1c4f0af3f1144aa298d604a1e633c720
Source noteuspto-grants-1993_03