Реакция #1960508

ord-7fed7daebff44f0f89356262ba76d98b

Уравнение реакции

CCCC1CCC(C2C=Cc3c(c(F)c(F)c4cc(OCC)ccc34)O2)CC1
8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-3H-benzo[f]chromene
CCCC1CCC(C2CCc3c(c(F)c(F)c4cc(OCC)ccc34)O2)CC1
8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-2,3-dihydro-1H-benzo[f]chromene

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe reaction solution is filtered
  2. 2
    Другоеthe filtrate is evaporated to dryness
  3. 3
    ДругоеThe residue is recrystallised from ethyl acetate

Методика

5.1 g (13.1 mmol) of 8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-3H-benzo[f]chromene are hydrogenated at atmospheric pressure in THF and in the presence of Pd/C (5% of Pd). The reaction solution is filtered, and the filtrate is evaporated to dryness. The residue is recrystallised from ethyl acetate, giving 8-ethoxy-5,6-difluoro-3-(4-propylcyclohexyl)-2,3-dihydro-1H-benzo[f]chromene as a colourless solid (m.p. 158° C.).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08303844B2uspto-grants-2012_11