Reacción #1929014

ord-7de38795d58d4a14acea9041ea0f462f

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08945420B2uspto-grants-2015_02