Реакция #1960488

ord-2ac63e8aef864433a077c3bfb7db7e0d

Уравнение реакции

Cl
hydrochloric acid
C#CC(Oc1cc2c(c(F)c1F)OCCC2)C1CCC(CCC)CC1
7,8-difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]-chroman
[F-].[K+]
potassium fluoride
O
water
CCCC1CCC(C2C=Cc3c4c(c(F)c(F)c3O2)OCCC4)CC1
5,6-difluoro-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ТемператураAfter cooling
  2. 2
    ЭкстракцияThe batch is extracted with MTBE
  3. 3
    Промывкаthe organic phase is washed with saturated sodium chloride solution
  4. 4
    ДругоеThe solution is dried
  5. 5
    Другоеevaporated to dryness
  6. 6
    ДругоеThe crude product is purified by column chromatography (SiO2, 1-chlorobutane)

Методика

6.0 g (17.2 mmol) of 7,8-difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]-chroman are heated at 200° C. for 6 h together with 2.0 g (34.4 mmol) of potassium fluoride in 55 ml of N,N-diethylaniline. After cooling, water is added, and the mixture is acidified using 25% hydrochloric acid. The batch is extracted with MTBE, and the organic phase is washed with saturated sodium chloride solution. The solution is dried using sodium sulfate and evaporated to dryness. The crude product is purified by column chromatography (SiO2, 1-chlorobutane), giving 5,6-difluoro-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene as a pale-brown oil.

Источник

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