Реакция #48818
ord-3d1941a623324da78a0d203e0cbd8d49
Уравнение реакции
Реагенты
Нет
Растворители
Условия реакции
Температура
45°CELSIUS
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Температураbefore cooling back to RT
- 2ЭкстракцияThe aqueous layer was then extracted with ethyl acetate (5×30 mL)
- 3Сушкаthe combined organic layers were dried (MgSO4)
- 4workup.ADDITIONtreated with activated charcoal
- 5Фильтрацияfiltered
- 6Другоеevaporated
- 7ДругоеThe residue was purified by chromatography
- 8Промывкаeluting with 67%-100% ethyl acetate in hexanes
Методика
2-Chloroacrylonitrile (3.41 mL, 42.59 mmol) was added at RT to a stirring solution of N-isopropylhydrazine hydrochloride (4.71 g, 42.6 mmol), potassium carbonate (11.8 g, 85.2 mmol) in water (50 mL). The reaction was warmed to 45° C. for 4 hours before cooling back to RT. The aqueous layer was then extracted with ethyl acetate (5×30 mL) and the combined organic layers were dried (MgSO4), treated with activated charcoal, filtered and evaporated. The residue was purified by chromatography, eluting with 67%-100% ethyl acetate in hexanes, to afford the title compound (3.08 g, 58%) as a 6:1 mixture of authentic product to regioisomeric product as an oil. The material was used without further purification.