Reacción #674299

ord-5da05256bf684a199f4b4b90ac122670

Ecuación de reacción

C=C1CCN(C(=O)OC(C)(C)C)CC1
tert-butyl 4-methylenepiperidine-1-carboxylate
O=C(Cl)C(Cl)(Cl)Cl
2,2,2-trichloroacetyl chloride
[Cl-].[NH4+]
NH4Cl
N#N
N2
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)C2
tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate
Rendimiento 15.0%

Disolventes

Condiciones de reacción

Temperatura
15°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroTo the mixture thus obtained
  2. 2
    workup.STIRRINGThe mixture was stirred at room temperature overnight
  3. 3
    workup.ADDITIONafter addition
  4. 4
    workup.STIRRINGTo the reaction mixture stirred in an external ice-bath
  5. 5
    workup.ADDITIONAfter addition
  6. 6
    workup.STIRRINGthe mixture was stirred at room temperature for 4 h
  7. 7
    Filtraciónfiltered
  8. 8
    Otroto remove the solid
  9. 9
    OtroThe phases were separated
  10. 10
    ExtracciónThe aqueous phase was extracted with EtOAc
  11. 11
    LavadoThe combined organic phase was washed with brine
  12. 12
    Secadodried over anhydrous Na2SO4
  13. 13
    Concentraciónconcentrated
  14. 14
    Otroto give the residue which
  15. 15
    Otrowas purified by CombiFlash (40 g silica gel column, EtOAc/Hexane: 0-40%)

Procedimiento

To a flame-dried RB flask with tert-butyl 4-methylenepiperidine-1-carboxylate (2.96 g, 15 mmol, 1.0 equiv) and Zn/Cu couple (6.54 g, 172.5 mmol, 11.5 equiv) under vacuum, t-BuOMe (60 mL) was charged and refilled the flask with N2 balloon. To the mixture thus obtained stirred at 15° C., a solution of 2,2,2-trichloroacetyl chloride in DME (20 mL) was added dropwise. The mixture was stirred at room temperature overnight after addition. To the reaction mixture stirred in an external ice-bath, a saturated solution of NH4Cl (60 mL) was added slowly and carefully (especially the first few drops). After addition, the mixture was stirred at room temperature for 4 h, filtered to remove the solid. The phases were separated. The aqueous phase was extracted with EtOAc. The combined organic phase was washed with brine, dried over anhydrous Na2SO4, concentrated to give the residue which was purified by CombiFlash (40 g silica gel column, EtOAc/Hexane: 0-40%) to afford 619 mg (15%) of tert-butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09226923B2uspto-grants-2016_01