Реакция #65741

ord-700ec23cf79745269df3f782f824b98b

Реагенты

Нет

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеthe mixture was reacted at 120° C. for 1.5 hours
  2. 2
    ДругоеThe reaction residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane 2:1)

Методика

Dimethyl fumarate (781 mg; 1.1 eq.) was added to 5-ethoxyoxazole (557.3 mg; 4.9 mmol), and the mixture was reacted at 120° C. for 1.5 hours. The reaction residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane 2:1), to give crude crystals of the title compound. Yield: 730 mg (70.2%). The crude crystals were recrystallized from dichloromethane-hexane, to give colorless plates.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05420275uspto-grants-1995_05