Reacción #40915
ord-68c8ac8859e74626b8a337ceb841d865
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted
- 2workup.ADDITIONafter adding water (80 ml)
- 3SecadoThe organic phase was dried over sodium sulfate
- 4Concentraciónconcentrated by evaporation in vacuo
- 5Otrothe 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 extracted, after adding water (80 ml), 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.