تفاعل #65860
ord-b99914fe8ca64664a127549fdc50c61c
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةunder reflux for 6 hours
- 2درجة الحرارةIt was then cooled
- 3أخرىthe precipitate formed
- 4ترشيحwas filtered off
- 5غسيلThe filtrate was washed with 5% by weight aqueous sodium hydrogen-sulphite solution and saturated aqueous sodium hydrogen-carbonate solution
- 6تركيزconcentrated on a rotary evaporator
- 7workup.DISSOLUTIONThe remaining residue was dissolved in 300 ml of diethyl ether
- 8workup.ADDITION100 ml of 1 N sodium hydroxide solution were added at room temperature
- 9أخرىthe phases were separated
- 10غسيلthe organic phase was washed with saturated aqueous ammonium chloride solution
- 11تجفيفdried over magnesium sulphate
- 12workup.DISTILLATIONsubjected to fractional distillation under vacuum
الإجراء التجريبي
50 g of 2(1-chloro-2,2,2-trifluoroethyl)-2-(trifluoromethyl)-5-formyl-1,3-benzodioxole were dissolved in 500 ml of methylene chloride, and 53 g of 70% by weight m-chloroperbenzoic acid were added. The reaction mixture was stirred under reflux for 6 hours. It was then cooled and the precipitate formed was filtered off. The filtrate was washed with 5% by weight aqueous sodium hydrogen-sulphite solution and saturated aqueous sodium hydrogen-carbonate solution and concentrated on a rotary evaporator. The remaining residue was dissolved in 300 ml of diethyl ether, and 100 ml of 1 N sodium hydroxide solution were added at room temperature. When the reaction was complete, the phases were separated and the organic phase was washed with saturated aqueous ammonium chloride solution, dried over magnesium sulphate and subjected to fractional distillation under vacuum. The yield was 26 g (=54% of theory) and the boiling point was 95° C. at 0.07 mbar. 19F NMR: -68.6 and -81.6 ppm. 1H NMR: 4.70 ppm.