Reacción #4994

ord-ee847813e8e14c88ba9cb5b8597ec847

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe mixture was heated
  2. 2
    Temperaturato reflux for 4 hours
  3. 3
    OtroAfter evaporation of methanol, water
  4. 4
    workup.ADDITIONwas added to the residue
  5. 5
    ExtracciónThe aqueous solution was extracted with ethylacetate
  6. 6
    OtroAfter evaporation of ethylacetate
  7. 7
    Otrothe residue was purified by column chromatography(benzene:ether=1.1)

Procedimiento

0.9 g of 3-ethylcarbonyl-5-[(2,4-dichlorophenoxy)methyl]-1,2,4-oxadiazole and 0.21 g of hydroxyamine hydrochloride were added to 10 ml of methanol. The mixture was heated to reflux for 4 hours. After evaporation of methanol, water was added to the residue. The aqueous solution was extracted with ethylacetate. After evaporation of ethylacetate, the residue was purified by column chromatography(benzene:ether=1.1) to provide 0.80 g of the desired product(yield: 85.0%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05242890uspto-grants-1993_09