Реакция #6155

ord-ec56bca52c65474f938fae5cfb0fea03

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe catalyst was filtered off
  2. 2
    Другоеthe solution was evaporated
  3. 3
    ДругоеAfter recrystallization

Методика

M)c) 8 g of an isomer mixture of tetrahydro-3-hexyl-4-oxo-(R)-6-undecyl-2H-pyran-2-one were dissolved in 2 l of ethyl acetate and 3 g of PtO2 were added. The mixture was then hydrogenated (50 bar) for 12 hours. The catalyst was filtered off and the solution was evaporated. After recrystallization there were obtained 7 g of (3S,4S,6R)-tetrahydro-3-hexyl-4-hydroxy-6-undecyl-2H-pyran-2-one, m.p. 108°-109° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05246960uspto-grants-1993_09