Реакция #2146781

ord-3f07b8b1c8f34afdafbc3f724656e5ef

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураthe reaction was refluxed for 3 h
  2. 2
    Концентрированиеwas concentrated onto silica gel in vacuo
  3. 3
    Промывкаeluted through a short silica plug (sequential elution—hexane, 10% diethyl ether in hexanes)

Методика

To a stirred suspension of 4-iodo-1H-pyrazole (1.50 g, 7.73 mmol) and potassium carbonate (2.67 g, 19.3 mmol) in acetone was added benzyl bromide (0.96 mL, 8.07 mmol) and the reaction was refluxed for 3 h. After cooling to room temperature the mixture was concentrated onto silica gel in vacuo and eluted through a short silica plug (sequential elution—hexane, 10% diethyl ether in hexanes) to provide the title compound as a white solid (2.12 g, 97% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08278290B2uspto-grants-2012_10