Reacción #66162

ord-2fab76d5241947dead68d408eaf254c6

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    Concentraciónthe mixture is concentrated
  3. 3
    Otrothe residue is initially pre-purified by flash chromatography on silica gel (mobile phase: gradient cyclohexane/ethyl acetate 1:1 ethyl acetate/ethanol 9:1)
  4. 4
    OtroThe product obtained in this manner
  5. 5
    workup.DISTILLATIONis then subjected to fine purification by distillation under reduced pressure (1 mbar, bath temperature 200° C.)

Procedimiento

37.4 g (226 mmol) of ethyl pyridin-3-ylacetate in 100 g (679 mmol) of dimethylformamide diethyl acetal are heated at 100° C. overnight. After cooling, the mixture is concentrated and the residue is initially pre-purified by flash chromatography on silica gel (mobile phase: gradient cyclohexane/ethyl acetate 1:1 ethyl acetate/ethanol 9:1). The product obtained in this manner is then subjected to fine purification by distillation under reduced pressure (1 mbar, bath temperature 200° C.).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524699B2uspto-grants-2013_09