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HRID 215713作成日:2026年10月23日

Diisopropylamine → Benzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-

https://huagongshe.com/ja/reaction/215713

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Dimethyl DisulfideHCID 12232—
反応物alpha,alpha,alpha,3-TetrafluorotolueneHCID 67867—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Benzene, 1-fluoro-2-(methylthio)-3-(trifluoromethyl)-HCID 4145933—

反応条件

温度-78 °C

反応手順

Under an atmosphere of inert gas, 32.8 ml (1.6 M in hexane, 52.5 mmol) of n-butyllithium were added dropwise to a solution, cooled to 0° C., of 7.77 ml (55 mmol) of diisopropylamine in 100 ml of anhydrous THF, and after 10 minutes of stirring the solution was cooled to −78° C. 8.21 g (50 mmol) of 3-fluorobenzotrifluoride were added at this temperature, and the reaction mixture was stirred at this temperature for 1 h. 4.21 ml (55 mmol) of dimethyl disulfide were then added dropwise. Within about 3 h, the reaction mixture had warmed to room temperature (RT), and it was then once more cooled to 0° C. At this temperature, 10 ml of water were added dropwise, and the reaction mixture was concentrated to about ¼ of its volume. The residue was taken up in water and dichloromethane, the phases were separated and the organic phase was washed successively with water, 10 percent strength hydrochloric acid, water, saturated aqueous NaHCO3 solution, water and saturated aqueous NaCl solution and dried over sodium sulfate and filtered. The solvent was removed and the residue was rectified under reduced pressure. This gave 8 g of 1-fluoro-2-methylthio-3-(trifluoromethyl)benzene of a boiling point of 68° C. at 6 mm Hg.

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-f03c3b23adf643bfa7c351188a29ec10
出典メモuspto-grants-2012_06