Реакция #1605775
ord-4184a2ab89c04c4d956d997123143e0a
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe reaction was cooled to room temperature
- 2Температураthe reaction mixture was then heated at 70° C. for 2 hrs
- 3ТемператураAfter cooling
- 4Промывкаthe resulting solution was washed with ether
- 5Другоеwas basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3
- 6Экстракцияthen extracted with ether (5×100 mL)
- 7СушкаThe organic layer was dried over MgSO4
- 8Фильтрацияfiltered
- 9Другоеevaporated
Методика
To a solution of 18 g of crude 2-(5-methylpyridin-2-yl)acetonitrile in dry THF (100 mL) was added dropwise Borane-tetrahydrofuran complex (1.0 M in THF, 232 mL, 232.5 mmol, 4 eq) at 0° C. under N2 atmosphere. The reaction mixture was then heated to 60° C. overnight. The reaction was cooled to room temperature, aq.HCl (6 N, 40 mL) was added carefully and the reaction mixture was then heated at 70° C. for 2 hrs. After cooling, water was added and the resulting solution was washed with ether. The aqueous layer was basified with aq. NaOH (10 N) at 0° C. and saturated with K2CO3 then extracted with ether (5×100 mL). The organic layer was dried over MgSO4, filtered and evaporated to give 7.6 g of crude 2-(5-methylpyridin-2-yl)ethanamine. (96% crude yield)