Reacción #49686

ord-95f5bb33bf7440c88b09193ba4fb2a51

Condiciones de reacción

Temperatura
30°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooling
  2. 2
    workup.STIRRINGby stirring for one hour at 80° C
  3. 3
    workup.ADDITIONwas added
  4. 4
    Extracciónthe aqueous layer was further extracted three times with chloroform
  5. 5
    Secadothe mixture was dried over anhydrous magnesium sulfate
  6. 6
    Concentraciónconcentrated under reduced pressure
  7. 7
    Otrothe residue formed
  8. 8
    Otrowas recrystallized from a mixture of chloroform and n-hexane

Procedimiento

In 20 ml of dimethylformamide (DMF) was suspended 96 mg of 60% sodium hydride under ice-cooling, 5 ml of a DMF solution of 548 mg of 2-benzylidenehydrazono-1-methoxycarbonylmethylimidazolidin-4-one was gradually added to the suspension. After stirring the mixture for one hour at 30° C., 254 mg of ethyl chloroacetate was gradually added dropwise thereto, followed by stirring for one hour at 80° C. After cooling the reaction mixture, water and chloroform was added thereto to distribute the mixture between water and chloroform, and the aqueous layer was further extracted three times with chloroform. The organic layer was combined with the extract, the mixture was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and the residue formed was recrystallized from a mixture of chloroform and n-hexane to obtain 320 mg of 2-benzylidenehydrazono-3-ethoxycarbonylmethyl-1-methoxycarbonylmethylimidazolidin-4-one.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05422360uspto-grants-1995_06