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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005480Generated: October 31, 2026

Carbon Dioxide → 2,3-Dichloro-6-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/1005480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant3,4-DichlorobenzotrifluorideHCID 9481—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,3-Dichloro-6-(trifluoromethyl)benzoic acidHCID 1165180388.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

83.4 g of 3,4-dichlorobenzotrifluoride was dissolved in 800 ml of dried tetrahydrofuran, and 250 ml of hexane solution of n-butyl lithium(1.6 mol/1) was added to the solution dropwise over 15 minutes at -78° C. under nitrogen atmosphere. Following to stirring the solution for 2 hours at -78° C., 50 g of dry ice was then gradually added to the solution at the same temperature. After elevating the temperature of the solution up to room temperature, 250 ml of cold water was added to the solution to separate the resulting solution, and the aqueous layer obtained was adjusted to an acidic condition of a pH value of 1 with concentrated hydrochloric acid while cooling. Then, the aqueous layer was extracted with ether, and the extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled out under reduced pressure, and the oily residue obtained was crystalized with n-hexane, washed, filtered, and dried to obtain 89 g of the title compound(mp. 88-89° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054605
Source datasetuspto-grants-2000_04
ORD IDord-f2d89c5c41894bbe9aa355a5eba760e0
Source noteuspto-grants-2000_04