تفاعل #1960494

ord-89592df4ae1148a2b2851dd0939ee196

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling
  2. 2
    استخلاصThe batch is extracted with MTBE
  3. 3
    غسيلthe organic phase is washed with saturated sodium chloride solution
  4. 4
    أخرىThe solution is dried
  5. 5
    أخرىevaporated to dryness
  6. 6
    أخرىThe crude product is purified by column chromatography (SiO2, 1-chlorobutane:pentane=4:1)

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08303844B2uspto-grants-2012_11