Реакция #5411

ord-be24221918f44d34a8f5c8d9a0afeeda

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling
  2. 2
    Промывкаthe reaction mixture was washed with an aqueous sodium sulfite solution
  3. 3
    Сушкаdried over anhydrous magnesium sulfate
  4. 4
    ДругоеThe solvent was removed under reduced pressure

Методика

A solution of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)thiazolidine (1.6 g) and N-bromosuccinimide (2 g) in chloroform (50 ml) was refluxed for 10 hours. After cooling, the reaction mixture was washed with an aqueous sodium sulfite solution and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was subjected to column chromatography to give 0.9 g of 2-ethoxycarbonylimino-3-(3-trifluoromethylphenyl)-5-bromothiazoline (Compound No. 30).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05244863uspto-grants-1993_09