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HRID 2081329作成日:2026年10月27日

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

https://huagongshe.com/reaction/2081329

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物Hydrochloric AcidHCID 313—
反応物IodineHCID 807—
反応物MagnesiumHCID 5462224—
反応物1-Bromo-4-methoxy-2-(trifluoromethyl)benzeneHCID 14484727—
溶媒TetrahydrofuranHCID 8028—
生成物4-methoxy-2-(trifluoromethyl)benzoic AcidHCID 277529439.5%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05183934
出典データセットuspto-grants-1993_02
ORD IDord-314b0b1b98fc45a1b20a8bf062c2018f
出典メモuspto-grants-1993_02