Reaktion #54238

ord-6d71dec87d5b41af88f4e662ee15c4e6

Reaktionsgleichung

CC(c1ccccc1)C(Br)C(=O)c1ccccc1
2-Bromo-3-phenyl-butyrophenone
c1nc[nH]n1
1,2,4-triazole
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(c1ccccc1)C(C(=O)c1ccccc1)n1cncn1
title compound
CC(c1ccccc1)C(C(=O)c1ccccc1)n1cncn1
2-(1,2,4-Triazol-1-yl)-3-phenylbutyrophenone

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe solution was filtered
  2. 2
    Sonstigethe solvent removed in vacuo
  3. 3
    SonstigeRecrystallisation of the residue from ethanol/petroleum ether (60°-80°)

Vorschrift

2-Bromo-3-phenyl-butyrophenone (0.02 mol), 1,2,4-triazole (0.02 mol) and potassium carbonate (0.04 mol) were refluxed in methyl ethyl ketone (100 ml) for 36 hours. After cooling to room temperature, the solution was filtered and the solvent removed in vacuo. Recrystallisation of the residue from ethanol/petroleum ether (60°-80°) gave the title compound as a colourless solid, m.p. 166°-8°.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04147793uspto-grants-1979_04