Reacción #8621

ord-f6db860dab31434dab410e8efec808ed

Ecuación de reacción

Cl
HCl
C=C[CH2][Mg][Cl]
allyl magnesium chloride
COc1ccncc1
4-methoxypyridine
O=C(Cl)OCc1ccccc1
benzyl chloroformate
C=CCC1=CC(=O)CCN1C(=O)OCc1ccccc1
desired product
C=CCC1=CC(=O)CCN1C(=O)OCc1ccccc1
N-Cbz-6-allyl-2,3-dihydro-1H-pyridin-4-one

Disolventes

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathen cooled to −75° C.
  2. 2
    workup.WAITThe solution is held at −75° C. for 4 hours
  3. 3
    workup.ADDITIONis added
  4. 4
    Otroto quench
  5. 5
    Otrothe reaction
  6. 6
    OtroThe organic layer is isolated
  7. 7
    Otropurified over silica gel

Procedimiento

To a solution of 4-methoxypyridine (50 mL, 0.492 mol) in toluene (1 L) is added benzyl chloroformate (70.3 mL, 0.492 mol) at 0° C. The resulting mixture is stirred at 0° C. for 30 minutes then cooled to −75° C. and allyl magnesium chloride (295.5 mL, 0.591 mol) is added. The solution is held at −75° C. for 4 hours and allowed to warm to 0° C. at which point a solution of 20% HCl is added to quench the reaction. The organic layer is isolated and purified over silica gel to yield the desired product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087759B2uspto-grants-2006_08