Reacción #469442

ord-4e930e5dba444dff9fd9106338b9e3eb

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaunder reflux for 3 hours
  3. 3
    workup.DISTILLATIONthe solvent was distilled off

Procedimiento

1-(4-Bromophenyl)-3-(2-thienyl)-2-propen-1-one (3.0 g, 10.2 mmol) and hydrazine hydrate (1.0 g, 20 mmol) were added to ethanol (30 ml) and heated under reflux for 3 hours. After the mixture was allowed to cool to room temperature, the solvent was distilled off to obtain 3.0 g (98%) of the desired 3-(4-bromophenyl)-5-(2-thienyl)-pyrazoline in the form of a resinous material.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06310049B1uspto-grants-2001_10