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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 215714생성일: 2026년 10월 25일

Carbon Dioxide → HCID 66957735, 화합물

https://huagongshe.com/reaction/215714

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물WaterHCID 962—
반응물Benzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-HCID 4145933—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물HCID 66957735HCID 66957735—

반응 조건

온도-78 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193121B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-811825d1797540e0947d913cc770fae5
출처 메모uspto-grants-2012_06