Реакция #696697

ord-728138628f044e39bf42b12ad90f8c95

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe solvent was removed
  2. 2
    Другоеto leave a crude semi-solid which
  3. 3
    Другоеwas purified by column chromatography on silica

Методика

To the sodium salt of 2-nitroimidazole prepared above was added acetonitrile (50 ml), 15-crown-5-ether (3.5 ml, 14.3 mmol) and 4-bromo-2-methyl-2-butene (2 ml; 17.4 mmol). The mixture was stirred at RT for ca 16 h. and then the solvent was removed to leave a crude semi-solid which was purified by column chromatography on silica. The intermediate product, 1-(3-methyl-2-butenyl)-2-nitroimidazole (80% yield) was eluted using a mixture of petroleum ether (40-60)/ethyl acetate (ratio 4:1 respectively).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05997843uspto-grants-1999_12