Reacción #75617
ord-686052dff0074236bc1ad47101bb61b1
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturathe reaction solution was cooled
- 2Otroat 0° C. or less
- 3FiltraciónThe mixture was filtered through Celite
- 4Otroevaporated
- 5ExtracciónThe resulting residue was extracted with ethyl acetate
- 6LavadoThe extract was washed with brine
- 7Secadodried over anhydrous magnesium sulfate
- 8Filtraciónfiltered
- 9OtroThe filtrate was evaporated
Procedimiento
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.