Реакция #5214

ord-715795a169ab49eca88ae924fb7a34b7

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
  2. 2
    Другоеto leave a residue, which
  3. 3
    Другоеwas purified by column chromatography through silica gel
  4. 4
    Промывкаeluted with a 10:1 by volume mixture of ethyl acetate and methanol

Методика

20 ml of trifluoroacetic acid and 0.41 ml of trifluoromethanesulfonic acid were added, whilst ice-cooling, to a solution of 949 mg of 3-(4-methoxybenzylthio)pyrrolidin-2-one in 4 ml of anisole, and then the mixture was stirred at room temperature for 30 minutes. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure to leave a residue, which was purified by column chromatography through silica gel, eluted with a 10:1 by volume mixture of ethyl acetate and methanol, to give 728 mg of the title compound as an oil.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05242914uspto-grants-1993_09