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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081329Generated: October 26, 2026

Carbon Dioxide → 4-methoxy-2-(trifluoromethyl)benzoic Acid

https://huagongshe.com/reaction/2081329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
ReactantMagnesiumHCID 5462224—
Reactant1-Bromo-4-methoxy-2-(trifluoromethyl)benzeneHCID 14484727—
SolventTetrahydrofuranHCID 8028—
Product4-methoxy-2-(trifluoromethyl)benzoic AcidHCID 277529439.5%

Reaction Steps

Dry tetrahydrofuran (10 ml) was added to 3-trifluoromethyl-4-bromo-1-methoxybenzene (compound III) (4.4 g) and metallic magnesium (0.41 g) and thereto was further added a catalytic amount of iodine, followed by refluxing for 1.5 hours with stirring. After the temperature was returned to room temperature, to the mixture was slowly added dropwise a solution prepared by adding dry ice (30 g) to dry tetrahydrofuran (10 ml) at -40° C. or lower. The temperature was returned to room temperature and then the reaction was allowed to proceed for further 2 hours. Then, the reaction mixture was added to 1N hydrochloric acid (50 ml) to stop the reaction and repeatedly extracted with ethyl acetate. The ethyl acetate layer was sufficiently washed with water and dried by adding anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and then, the resulting solid was recrystallized from methylene chloride to obtain 2-trifluoromethyl-4-methoxybenzoic acid (compound IV, 1.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183934
Source datasetuspto-grants-1993_02
ORD IDord-314b0b1b98fc45a1b20a8bf062c2018f
Source noteuspto-grants-1993_02