Reacción #61692

ord-b304d4c32fef404f97a5da0ed3d58746

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    Otrothe solution is evaporated to dryness
  3. 3
    Extracciónthe residue is extracted with dichloromethane/water
  4. 4
    LavadoThe organic phase is washed with water
  5. 5
    Secadodried over magnesium sulfate (MgSO4)
  6. 6
    workup.DISTILLATIONthe solvent is distilled off
  7. 7
    OtroThe product is purified by recrystallization from diethyl ether

Procedimiento

13.4 g (0.056 mol) of methyl ester 3a, 11.65 g (0.084 mol) of tropenol, and 0.3 g of sodium are heated as a melt at 75 mbar for 4 hours over a bath of boiling water with occasional agitation. After cooling, the sodium residues are dissolved with acetonitrile, the solution is evaporated to dryness, and the residue is extracted with dichloromethane/water. The organic phase is washed with water, dried over magnesium sulfate (MgSO4), and the solvent is distilled off. The product is purified by recrystallization from diethyl ether. Yield: 11.40 g of white crystals (29% of theoretical yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07429600B2uspto-grants-2008_09