Réaction #1960490

ord-99a9c6d81ce54503a22202bff0fb1439

Équation de réaction

CC(C)OC(=O)/N=N/C(=O)OC(C)C
DIAD
Oc1cccc(F)c1F
2,3-difluorophenol
C#CC(O)CCCCC
1-octyn-3-ol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
C#CC(CCCCC)Oc1cccc(F)c1F
1-(1-ethynylhexyloxy)-2,3-difluorobenzene

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Lavagewashed with water
  2. 2
    ExtractionThe aqueous phase is extracted with MTBE
  3. 3
    Lavagethe combined organic phases are washed with saturated sodium chloride solution
  4. 4
    AutreThe solution is dried
  5. 5
    Autreevaporated to dryness
  6. 6
    AutreThe residue is purified by column chromatography (SiO2, 1-chlorobutane)

Mode opératoire

2.4 g (0.33 mol) of 2,3-difluorophenol are initially introduced in 1.2 l of THF together with 50.0 ml (0.34 mol) of 1-octyn-3-ol and 94.1 g (0.36 mol) of triphenylphosphine, and a solution of 76.1 ml (0.39 mol) of DIAD in 100 ml of THF is added dropwise. After 19 h at RT, the batch is diluted with MTBE and washed with water. The aqueous phase is extracted with MTBE, and the combined organic phases are washed with saturated sodium chloride solution. The solution is dried using sodium sulfate and evaporated to dryness. The residue is purified by column chromatography (SiO2, 1-chlorobutane), giving 1-(1-ethynylhexyloxy)-2,3-difluorobenzene as a colourless oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08303844B2uspto-grants-2012_11