Реакция #54238

ord-6d71dec87d5b41af88f4e662ee15c4e6

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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°.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04147793uspto-grants-1979_04