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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-Bromo-4-methoxy-2-(trifluoromethyl)benzene | HCID 14484727 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-methoxy-2-(trifluoromethyl)benzoic Acid | HCID 2775294 | 39.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05183934 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-314b0b1b98fc45a1b20a8bf062c2018f |
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| Source note | uspto-grants-1993_02 |
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