Réaction #1929014

ord-7de38795d58d4a14acea9041ea0f462f

Équation de réaction

CCCC1CCC(/C(F)=C(\F)[Si](CC)(CC)CC)CC1
[(Z)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]triethylsilane
O
water
CCCC[N+](CCCC)(CCCC)CCCC.[F-]
TBAF
CCCC1CCC(/C(F)=C\F)CC1
1-((E)-1,2-difluorovinyl)-4-propylcyclohexane

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed a number of times with water
  2. 2
    ExtractionThe aqueous phases are extracted with MTBE
  3. 3
    Lavagethe combined organic phases are washed with water and saturated sodium chloride solution
  4. 4
    AutreThe solution is dried
  5. 5
    Concentrationconcentrated under reduced pressure
  6. 6
    AutreThe residue is purified by column chromatography (SiO2, pentane)

Mode opératoire

34.6 g (0.11 mol) of [(Z)-1,2-difluoro-2-(4-propylcyclohexyl)vinyl]triethylsilane are refluxed for 20 h in 900 ml of THF together with 45 ml of water and 160 ml of TBAF (0.16 mol, 1 M soln. in THF). The batch is diluted with MTBE and washed a number of times with water. The aqueous phases are extracted with MTBE, and the combined organic phases are washed with water and saturated sodium chloride solution. The solution is dried using sodium sulfate and concentrated under reduced pressure. The residue is purified by column chromatography (SiO2, pentane), giving 1-((E)-1,2-difluorovinyl)-4-propylcyclohexane as a colourless oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08945420B2uspto-grants-2015_02