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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005484Generated: October 30, 2026

Carbon Dioxide → 3-Chloro-2-fluoro-6-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1005484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHexaneHCID 8058—
Reactant4-Chloro-3-fluorobenzotrifluorideHCID 2736545—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-2-fluoro-6-(trifluoromethyl)benzoic acidHCID 277375494%

Reaction Conditions

Temperature-78 °C

Reaction Steps

77.0 g of 3-fluoro-4-chlorobenzotrifluoride was dissolved in 750 ml of dried tetrahydrofuran, and to the solution, 250 ml of hexane solution of n-butyl lithium (1.6 mol/l) was added dropwise over 15 minutes at -78° C. under a nitrogen atmosphere. After stirring the solution at -78° C. for 2 hours. 50 g of dry ice was gradually added to the solution at the same temperature. After elevating the temperature of the solution up to room temperature, 500 ml of ice water was added to the solution to separate the resulting solution. While cooling down the aqueous layer, the layer was adjusted to a pH value of 1 with concentrated hydrochloric acid. The aqueous layer was then extracted with ether, washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled under reduced pressure, and the oily residue obtained was crystalized with n-hexane, followed by a filtration and then dried to obtain 88.4 g of the title compound(mp. 92-93° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054605
Source datasetuspto-grants-2000_04
ORD IDord-8b85ed6de7204fdd82bd1c047d044d6c
Source noteuspto-grants-2000_04