Reacción #644694

ord-a348109e4acb49f68e13e71a6cc0b4ca

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 in vacuo
  4. 4
    Otrothe product was obtained in the form of a white solid

Procedimiento

40% aqueous dimethylamine solution (85 ml, 0.67 mol), 1,4-dioxa-spiro[4.5]decane-8-carbaldehyde 2 (240 g, 0.141 mol) and potassium cyanide (22.05 g, 0.338 mol) were added, while cooling with ice, to a mixture of 4N hydrochloric acid (37 ml) and methanol (22 ml). The mixture was stirred for 4 d at room temperature and then, after addition of water (80 ml), extracted with diethyl ether (4×100 ml). The organic phase was dried over sodium sulfate and concentrated in vacuo, and the product was obtained in the form of a white solid.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08058475B2uspto-grants-2011_11