Реакция #710491
ord-f5a02f319c614510b25985e63fc3ec89
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ЭкстракцияThe aequeous phase was extracted three times by 300 mL of ethyl acetate
- 2Промывкаthe organic phase was successively washed with brine, water
- 3Сушкаdried over magnesium sulfate
- 4ДругоеAfter evaporation of the solvent under vacuum 8.5 g of yellow oil
- 5Другоеwere obtained
- 6ФильтрацияAfter trituration in diisopropyl ether and filtration 6.8 g (80%) of 2-(3,5-dichloropyridin-2-yl)-2,2-difluoroethanol (Int-9)
- 7Другоеwere obtained as a white solid
- 8ДругоеMp (melting point)=56° C. (M+1)=228
Методика
To a solution of 10 g (37 mmol) of ethyl (3,5-dichloropyridin-2-yl)(difluoro)acetate (Int-7) in 60 mL of ethanol, were added portionwise at 0° C., 1.05 g (27.7 mmol) of sodium borohydride. The reaction mixture was stirred below 10° C. for 2 hours. 30 mL of 1 N HCl were then slowly added followed by 500 mL of water. The aequeous phase was extracted three times by 300 mL of ethyl acetate and the organic phase was successively washed with brine, water and dried over magnesium sulfate. After evaporation of the solvent under vacuum 8.5 g of yellow oil were obtained. After trituration in diisopropyl ether and filtration 6.8 g (80%) of 2-(3,5-dichloropyridin-2-yl)-2,2-difluoroethanol (Int-9) were obtained as a white solid. Mp (melting point)=56° C. (M+1)=228. 19F-NMR (235 MHz, CDCl3) δ (ppm): −105.85 (CF2).