Reacción #820259

ord-5a09c94650a14b8baa592ca524c5e8f3

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
    Otroevaporated under a vacuum
  4. 4
    Otrothe product obtained as a white solid

Procedimiento

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

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07589113B2uspto-grants-2009_09