Reacción #75617

ord-686052dff0074236bc1ad47101bb61b1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe reaction solution was cooled
  2. 2
    Otroat 0° C. or less
  3. 3
    FiltraciónThe mixture was filtered through Celite
  4. 4
    Otroevaporated
  5. 5
    ExtracciónThe resulting residue was extracted with ethyl acetate
  6. 6
    LavadoThe extract was washed with brine
  7. 7
    Secadodried over anhydrous magnesium sulfate
  8. 8
    Filtraciónfiltered
  9. 9
    OtroThe 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699870B2uspto-grants-2004_03