Reacción #11381
ord-bb30373df9eb45569b1a021302201d7c
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1ExtracciónThe solution is then extracted with 200 ml of ether
- 2Lavadothe organic phase is washed three times with water
- 3SecadoAfter drying over magnesium sulphate
- 4Otrothe ether is evaporated off
Procedimiento
A mixture composed of 0.1 mol (15.85 g) of 2-chloro-3-nitropyridine and 0.1 mol (11.50 ml) of cyclohexylamine is heated at 120° C. for 4 hours in 250 ml of DMF in the presence of potassium carbonate (13.81 g). The solution is then extracted with 200 ml of ether and the organic phase is washed three times with water. After drying over magnesium sulphate, the ether is evaporated off.