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HRID 215714作成日:2026年10月26日

Carbon Dioxide → 2-Fluoro-3-(methylthio)-4-(trifluoromethyl)benzoic acid

https://huagongshe.com/reaction/215714

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WaterHCID 962—
反応物Benzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-HCID 4145933—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物2-Fluoro-3-(methylthio)-4-(trifluoromethyl)benzoic acidHCID 66957735—

反応条件

温度-78 °C

反応手順

Under an atmosphere of inert gas, 27.5 ml (1.6 M in hexane, 44 mmol) of n-butyllithium were added dropwise to a solution, cooled to −78° C., of 7.98 g (38 mmol) of 1-fluoro-2-methylthio-3-(trifluoromethyl)benzene in 60 ml of anhydrous THF, where the temperature of the reaction mixture should not exceed −65° C. The mixture was stirred at −78° C. for 3 h, and at this temperature a carbon dioxide stream was then introduced such that the temperature of the reaction mixture did not exceed −45° C. The mixture was then warmed to RT and then once more cooled to 0° C. For work-up, water was added dropwise at this temperature until the precipitate formed had dissolved. Diethyl ether was added, and the organic phase was extracted three times with water. The combined aqueous phases were acidified with 10 percent strength hydrochloric acid. The aqueous phase was extracted repeatedly with dichloromethane, the combined organic phases were washed with saturated aqueous NaCl solution and dried over sodium sulfate and the filtrate was then freed from the solvent. The crude product obtained in this manner was then recrystallized from gasoline (80-110° C.)/ethyl acetate. This gave 6.8 g of 2-fluoro-3-methylthio-4-(trifluoromethyl)benzoic acid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193121B2
出典データセットuspto-grants-2012_06
ORD IDord-811825d1797540e0947d913cc770fae5
出典メモuspto-grants-2012_06