반응 #1960494

ord-89592df4ae1148a2b2851dd0939ee196

반응 방정식

Cl
hydrochloric acid
C#CC(Oc1cc2c(c(F)c1F)OC(CCCCC)CC2)C1CCC(CCC)CC1
7,8-difluoro-2-pentyl-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman
[F-].[K+]
potassium fluoride
O
water
CCCCCC1CCc2c3c(c(F)c(F)c2O1)OC(C1CCC(CCC)CC1)C=C3
5,6-difluoro-3-pentyl-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도After cooling
  2. 2
    추출The batch is extracted with MTBE
  3. 3
    세척the organic phase is washed with saturated sodium chloride solution
  4. 4
    기타The solution is dried
  5. 5
    기타evaporated to dryness
  6. 6
    기타The crude product is purified by column chromatography (SiO2, 1-chlorobutane:pentane=4:1)

실험 절차

9.7 g (23.2 mmol) of 7,8-difluoro-2-pentyl-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman are heated at 200° C. for 6 h together with 2.7 g (46.5 mmol) of potassium fluoride in 75 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:pentane=4:1), giving 5,6-difluoro-3-pentyl-8-(4-propylcyclohexyl)-1,2,3,8-tetrahydropyrano[3,2-f]chromene as a pale-brown oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08303844B2uspto-grants-2012_11