Reaktion #607448

ord-b9cfe71ab0de4373b6ab9dda6a18135a

Reaktionsgleichung

C=CCCCC=O
hex-5-enal
C[Si](C)(C)C(F)(F)F
trimethyl(trifluoromethyl)silane
C=CCCCC(O)C(F)(F)F
1,1,1-trifluorohept-6-en-2-ol
Ausbeute 31.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe ice bath was removed
  2. 2
    workup.ADDITIONUpon complete transformation of the starting material the reaction mixture was treated with 2M HCl
  3. 3
    workup.ADDITIONThen, 50 mL of Et2O was introduced
  4. 4
    Sonstigethe layers were separated
  5. 5
    ExtraktionThe aqueous fraction was additionally extracted with Et2O
  6. 6
    Waschenthe combined organic phases were washed sequentially with a saturated aqueous NaHCO3 solution, water, and brine
  7. 7
    TrocknenAfter drying with MgSO4 and filtration the solvent
  8. 8
    Sonstigewas removed under reduced pressure
  9. 9
    Sonstigethe resultant crude residue was purified by column chromatography (silica gel, pentane/Et2O, v/v=8/2)
  10. 10
    workup.ADDITIONFractions containing the pure compound
  11. 11
    Sonstigewere collected
  12. 12
    Einengenconcentrated in vacuo

Vorschrift

To a ice-bath cooled solution of hex-5-enal (500 mg, 4.331 mmol) and trimethyl(trifluoromethyl)silane (0.74 g, 5.13 mmol, 1.2 equiv.) in THF (10 mL) was added tetrabutylammonium hydrofluoride (10 mg, 0.04 mmol). The ice bath was removed and the reaction progress was monitored via GCMS and 1H NMR. Upon complete transformation of the starting material the reaction mixture was treated with 2M HCl and stirred for an additional 2 h. Then, 50 mL of Et2O was introduced and the layers were separated. The aqueous fraction was additionally extracted with Et2O and the combined organic phases were washed sequentially with a saturated aqueous NaHCO3 solution, water, and brine. After drying with MgSO4 and filtration the solvent was removed under reduced pressure and the resultant crude residue was purified by column chromatography (silica gel, pentane/Et2O, v/v=8/2). Fractions containing the pure compound were collected and concentrated in vacuo to give 1,1,1-trifluorohept-6-en-2-ol (225 mg, 31% yield) as a yellow oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09326513B2uspto-grants-2016_05