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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613966Generated: November 3, 2026

1-Chloro-4-(trifluoromethyl)benzene → 4-(Trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1613966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
ReactantSodium CarbonateHCID 10340—
ReactantHCID 178418416HCID 178418416—
Catalyst1,4-Bis(diphenylphosphino)butaneHCID 82124—
CatalystHCID 178418390HCID 178418390—
SolventWaterHCID 962—
Product4-(Trifluoromethyl)benzoic acidHCID 9966265.6%

Reaction Conditions

Temperature180 °C

Reaction Steps

In an autoclave made of glass were placed 180.6 g of parachlorobenzotrifluoride, 0.64 g of 5% palladium-carbon, 4.3 g of 1,4-bisdiphenylphosphinobutane and 21.2 g of sodium carbonate. The air in the autoclave was replaced with carbon monoxide introduced thereinto several times, after which carbon monoxide was further introduced to adjust its pressure therein to 10 kg/cm2. The reaction was carried out with stirring for 8 hours at 180° 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 101 g of paratrifluoromethylbenzoic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194631
Source datasetuspto-grants-1993_03
ORD IDord-7e26addbca144f9293f7dea343edc70d
Source noteuspto-grants-1993_03