Реакция #50115

ord-bf7906f994d34b849386db5656fd0255

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto reflux for 24 h
  2. 2
    ТемператураAfter cooling
  3. 3
    Экстракцияextracted with ether (3×30 cm3)
  4. 4
    Сушкаdried over MgSO4
  5. 5
    Фильтрацияfiltered
  6. 6
    Другоеevaporated down
  7. 7
    ДругоеThe crude product was purified by flash chromatography on silica (eluent: ether/petroleum ether=1/99)
  8. 8
    ДругоеThe following were isolated (
  9. 9
    Промывкаin the order of elution):

Методика

1.60 g (6.62 mmol) of epoxide 2j and 2 cm3 (25 mmol) of pyridine were heated to reflux for 24 h. After cooling, the mixture was acidified to pH=1 with 3N HCl, extracted with ether (3×30 cm3), dried over MgSO4, filtered and evaporated down. The crude product was purified by flash chromatography on silica (eluent: ether/petroleum ether=1/99). The following were isolated (in the order of elution): starting epoxide 2j, 0.40 g of transposition ketone 6a (Yld=40%), traces of 2-allyl-2,3-dichloro-3-cyclohexenone 7 (evidence based on GC/mass) and phenol 4f.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05424460uspto-grants-1995_06