Реакция #75617

ord-686052dff0074236bc1ad47101bb61b1

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe reaction solution was cooled
  2. 2
    Другоеat 0° C. or less
  3. 3
    ФильтрацияThe mixture was filtered through Celite
  4. 4
    Другоеevaporated
  5. 5
    ЭкстракцияThe resulting residue was extracted with ethyl acetate
  6. 6
    ПромывкаThe extract was washed with brine
  7. 7
    Сушкаdried over anhydrous magnesium sulfate
  8. 8
    Фильтрацияfiltered
  9. 9
    ДругоеThe 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06699870B2uspto-grants-2004_03