反応 #302895
ord-f03c3b23adf643bfa7c351188a29ec10
反応方程式
反応条件
後処理
- 1workup.STIRRINGthe reaction mixture was stirred at this temperature for 1 h
- 2workup.WAITWithin about 3 h
- 3温度the reaction mixture had warmed to room temperature (RT), and it
- 4温度was then once more cooled to 0° C
- 5濃縮the reaction mixture was concentrated to about ¼ of its volume
- 6その他dichloromethane, the phases were separated
- 7洗浄the organic phase was washed successively with water, 10 percent strength hydrochloric acid, water, saturated aqueous NaHCO3 solution, water and saturated aqueous NaCl solution
- 8乾燥dried over sodium sulfate
- 9ろ過filtered
- 10その他The solvent was removed
実験手順
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.