Reacción #94898

ord-ca363b7f65534cd6b1c78e535ccde923

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrosubstantially according to the procedure of Preparation 21
  2. 2
    OtroThe solid was recrystallized from hexane
  3. 3
    Otrogiving a small amount of material which
  4. 4
    OtroThe mother liquors were evaporated in vacuo
  5. 5
    Otroto give an oil which
  6. 6
    FiltraciónThe solid was filtered off

Procedimiento

The title compound was prepared from 3-phenyl-3-(4-nitrophenyl)propenoic acid via mixed anhydride formation using ethyl chloroformate, followed by reaction with 1-methyldecylamine, substantially according to the procedure of Preparation 21. The product was induced to solidify by trituration under hexane. The solid was recrystallized from hexane, giving a small amount of material which was discarded. The mother liquors were evaporated in vacuo to give an oil which solidified when stirred under acetonitrile. The solid was filtered off, giving a 51% yield of the title compound, m.p. 69°-71° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04342781uspto-grants-1982_08