Reacción #2467374

ord-f5df265d4af9460bb199ef33748953cc

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaat reflux overnight
  3. 3
    TemperaturaIt was cooled
  4. 4
    Otroevaporated to dryness
  5. 5
    OtroThe residue was purified by chromatography
  6. 6
    Lavadoeluted with a mixture of hexane and dichloromethane

Procedimiento

A mixture of 1-[2-chloro-4-(methylsulphenyl)phenyl]-3-cyclopropylprop-1-yn-3-one (1.39g) and ethyl chloro-oximidoacetate (0.84 g) in toluene was stirred and heated at reflux overnight. It was cooled and evaporated to dryness. The residue was purified by chromatography eluted with a mixture of hexane and dichloromethane, followed by ether to give ethyl 5-[2-chloro-4(methylsulphenyl)phenyl]-4-cyclopropylcarbonylisoxazole-3-carboxylate (compound 9, 0.72g) as an orange solid, m.p. 50° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05366957uspto-grants-1994_11