Reacción #40919

ord-85f0a1c8da154ceeb53790dd29fb205d

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with diethyl ether (4×100 ml)
  2. 2
    SecadoThe organic phase was dried over sodium sulfate
  3. 3
    Concentraciónconcentrated by evaporation in vacuo
  4. 4
    Otrothe product was obtained as a white solid

Procedimiento

40% aqueous dimethylamine solution (85 ml, 0.67 mole), 1,4-dioxa-spiro-[4.5]decane-8-carbaldehyde 5 (240 g, 0.141 mole) and potassium cyanide (22.05 g, 0.338 mole) were added while cooling with ice to a mixture of 4N hydrochloric acid (37 ml) and methanol (22 ml). The mixture was stirred for four days at room temperature and then, after adding water (80 ml), extracted with diethyl ether (4×100 ml). The organic phase was dried over sodium sulfate, concentrated by evaporation in vacuo, and the product was obtained as a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07728028B2uspto-grants-2010_06