Реакция #58450
ord-833207da9f374c3c903eabc45f79e847
Уравнение реакции
potassium hydroxide
(RS)-1-(tert-butyloxycarbonyl)-2-((5-(4-fluorophenyl)-furan-2-yl)carbonyl)piperidine
hydrazine hydrate
water
→
title compound
Выход 63.3%
(RS)-2-(5-(4-Fluorophenyl)-furan-2-ylmethyl)-piperidine
Выход 63.3%
Реактанты
Реагенты
Нет
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураthe mixture heated at 200° C. for 18 h
- 2Экстракцияextracted with diethyl ether (3×75 ml)
- 3СушкаThe combined organic extracts were dried (Na2SO4)
- 4Другоеevaporated in vacuo
Методика
To a solution of (RS)-1-(tert-butyloxycarbonyl)-2-((5-(4-fluorophenyl)-furan-2-yl)carbonyl)piperidine (2.0 g, 5.36 mmol) in diethylene glycol (20 g), was added hydrazine hydrate (0.31 ml, 5.36 mmol) and the resultant mixture heated at 100° C. for 30 min. After cooling to room temperature, potassium hydroxide (1.0 g, 17.8 mmol) was added and the mixture heated at 200° C. for 18 h. The reaction mixture was then poured into water (100 ml) and extracted with diethyl ether (3×75 ml). The combined organic extracts were dried (Na2SO4) and evaporated in vacuo to give the title compound as a brown oil (0.88 g, 63%).