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HRID 477271作成日:2026年10月23日

alpha,alpha,alpha,3-Tetrafluorotoluene → 2-Fluoro-6-(trifluoromethyl)benzoic acid

https://huagongshe.com/ja/reaction/477271

反応式

関与物質

役割名称HCID仕込み量
反応物alpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
反応物Dry ice diethyl etherHCID 86742199—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-Fluoro-6-(trifluoromethyl)benzoic acidHCID 688123—

反応条件

温度-78 °C

反応手順

A mixture of 3-fluorobenzotrifluoride (25.0 g, 0.15 mol) in tetrahydrofuran (200 ml) was cooled to -78° C. in a dry ice/acetone bath under nitrogen atmosphere. To this solution was added dropwise with rapid stirring N-butyl lithium (1.6M, 95.2 ml) at such rate that the temperature did not exceed -60° C. When the addition was complete, the mixture was allowed to stir at -78° C. for an additional five hours. The mixture was then poured over a slurry of dry ice/ether and allowed to come to room temperature. The solvent was removed by evaporation under reduced pressure to obtain a white solid residue. This solid was dissolved in a minimum amount of water, the solution was extracted with diethyl ether (2×100 ml) and the aqueous phase was acidified to pH 2 with dilute hydrochloric acid. An oil formed and this was dissolved in diethyl ether; the solution was washed several times with water and dried over magnesium sulfate. The solvent was removed by evaporation under reduced pressure to give a white solid. NMR analysis indicated this product was a mixture of the title compound and an isomer. A yield of 15.6 g (50 percent of theory) was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886883
出典データセットuspto-grants-1989_12
ORD IDord-ce0c886cd0244015ad87d4ea300fd7a9
出典メモuspto-grants-1989_12