Réaction #63936

ord-6c3a4db47a0a45f68dd1d01da747a525

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    TempératureAfter refluxing for a further 15 minutes the organic phase
  2. 2
    Températureafter cooling
  3. 3
    Autrewas separated
  4. 4
    AutreEvaporation
  5. 5
    Autregave a gum

Mode opératoire

2',4'-Dichloro-2-(1H-1,2,4-triazol-1-yl)prop-2-enophenone (0.27 g, 1.0 mMole) was added dropwise in 1,1,1-trichloroethane (2 ml) to a refluxing mixture of trimethylsulphoxonium iodide (0.33 g, 1.5 mMole), cetrimide (0.03 g), 1,1,1-trichloroethane (5 ml) and aqueous 2N sodium hydroxide (3 ml) with vigorous stirring over 2 minutes. After refluxing for a further 15 minutes the organic phase, after cooling was separated. Evaporation gave a gum, weight 0.11 g.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04767777uspto-grants-1988_08