Reacción #2170875
ord-04a432efd06f44e2a9d60ae5b3e21ffa
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Temperaturaunder reflux for 3 hours
- 2Filtraciónfiltered hot
- 3Otroto remove the inorganic sediment
- 4Otroevaporated in vacuo
- 5Otroto afford a thick syrup
- 6OtroThe latter was crystallized upon trituration in diethyl ether
- 7Otroa sample of the resultant solid was recrystallized from ethanol
Procedimiento
A mixture 3,4-dibenzyloxyphenacyl bromide (32.8 g.), N-[2-(4-carbamoylmethylphenoxy)ethyl]benzylamine (22.8 g.), anhydrous sodium carbonate (8.4 g.) and ethanol (1 liter) was boiled under reflux for 3 hours, then filtered hot to remove the inorganic sediment and evaporated in vacuo to afford a thick syrup. The latter was crystallized upon trituration in diethyl ether and a sample of the resultant solid was recrystallized from ethanol to give N-benzyl-N-(3,4-dibenzyloxybenzoyl)methyl-2-(4-carbamoylmethylphenoxy)ethylamine, m.p. 99°-101° C.