Reacción #217448
ord-2302910246ad4d5996efcd7c909db375
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroInto a 2 liter Erlenmeyer flask equipped
- 2TemperaturaThe mixture was heated to 120° C. for 4 hours
- 3Temperaturato cool to room temperature
- 4workup.STIRRINGto stir for 10 minutes
- 5Filtraciónwas then filtered
- 6Lavadowashed with 3×200 milliliter portions of methanol
- 7Otrodried at 60° C.
Procedimiento
Into a 2 liter Erlenmeyer flask equipped with magnetic stirring was charged stearylamine (118 g, 0.44 mol; obtained from Sigma-Aldrich) and ethyl cyanoacetate (ECA, 45.2 grams, 0.4 mol). The mixture was heated to 120° C. for 90 minutes, after which ethyl acetoacetate (EAA, 114 grams, 0.88 mol), piperidine (PIP; 70 grams, 0.82 mol), and dimethylformamide (DMF; 140 milliliters) were added. The mixture was heated to 120° C. for 4 hours. The mixture was then allowed to cool to room temperature and was poured slowly into well stirred methanol (1,200 milliliters), which contained concentrated hydrochloric acid (100 milliliters). The resulting suspension was allowed to stir for 10 minutes, and was then filtered and washed with 3×200 milliliter portions of methanol. The resulting solid was oven dried at 60° C. to give 91.3 grams of a beige powder at 57 percent yield.