Реакция #674298
ord-23e9ad5d83e14edba21f92d47c1fc3a9
Уравнение реакции
Условия реакции
Обработка
- 1Температураat reflux for 2 hrs
- 2Температураto warm to room temperature
- 3workup.STIRRINGstirred at room temperature for 1 h
- 4workup.STIRRINGThe mixture was then stirred
- 5Температураat reflux overnight (16 h)
- 6ТемператураThe mixture was cooled to room temperature
- 7workup.STIRRINGThe mixture was stirred for 10 min
- 8Фильтрацияfiltered
- 9Промывкаeluted with Hexane/EtOAc (100/100 mL)
- 10КонцентрированиеThe combined organic solution was concentrated
- 11Другоеto give the residue which
- 12Другоеwas purified by CombiFlash (100 g silica gel column, EtOAc/Hex=0-30%)
Методика
To a suspension of methyltriphenylphosphonium bromide (36.3 g, 101.6 mmol, 1.35 equiv) in ether (dry, 300 mL) was added potassium t-butoxide (11 g, 98 mmol, 1.3 equiv) in one portion at 0° C. under nitrogen balloon. The mixture was then stirred at reflux for 2 hrs. The hot reaction mixture was cooled to 0° C. with an external ice-bath and then a solution of tert-butyl 4-oxopiperidine-1-carboxylate (15 g, 75.3 mmol, 1.0 equiv) in ether (60 mL) was added dropwise. The mixture was allowed to warm to room temperature and stirred at room temperature for 1 h. The mixture was then stirred at reflux overnight (16 h). The mixture was cooled to room temperature and hexane (300 mL) was added. The mixture was stirred for 10 min, filtered and eluted with Hexane/EtOAc (100/100 mL). The combined organic solution was concentrated to give the residue which was purified by CombiFlash (100 g silica gel column, EtOAc/Hex=0-30%) to afford 14 g (yield 94%) of tert-butyl 4-methylenepiperidine-1-carboxylate as a colorless oil.