Реакция #75617
ord-686052dff0074236bc1ad47101bb61b1
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураthe reaction solution was cooled
- 2Другоеat 0° C. or less
- 3ФильтрацияThe mixture was filtered through Celite
- 4Другоеevaporated
- 5ЭкстракцияThe resulting residue was extracted with ethyl acetate
- 6ПромывкаThe extract was washed with brine
- 7Сушкаdried over anhydrous magnesium sulfate
- 8Фильтрацияfiltered
- 9ДругоеThe filtrate was evaporated
Методика
49.3 g of tert-butyl 4-methylene-1-piperidine carboxylate was added to a mixture of 157.2 g zinc-copper alloy and 500 ml diethyl ether, and 900 ml solution of 181.8 g trichloroacetyl chloride in dimethoxyethane was added dropwise thereinto over 5.5 hours. After stirred for 30 min, the reaction solution was cooled and saturated aqueous sodium bicarbonate was added thereto at 0° C. or less. The mixture was filtered through Celite and evaporated. The resulting residue was extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was evaporated, and the resulting residue was subjected to silica gel column chromatography to give 62.5 g of tert-butyl 1,1-dichloro-2-oxo-7-azaspiro[3.5]nonane-7-carboxylate.