Reacción #2170875

ord-04a432efd06f44e2a9d60ae5b3e21ffa

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaunder reflux for 3 hours
  2. 2
    Filtraciónfiltered hot
  3. 3
    Otroto remove the inorganic sediment
  4. 4
    Otroevaporated in vacuo
  5. 5
    Otroto afford a thick syrup
  6. 6
    OtroThe latter was crystallized upon trituration in diethyl ether
  7. 7
    Otroa 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04086272uspto-grants-1978_04