Reaktion #46031

ord-f2fa54f0504f43e49c4bb3af8257153a

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturby refluxing
  2. 2
    Temperaturunder heating for 2 hours
  3. 3
    ExtraktionThe aqueous layer was extracted with toluene, which
  4. 4
    workup.ADDITIONwas added to the organic layer
  5. 5
    Waschenthe organic layer was washed with a saturated salt solution
  6. 6
    Trocknendried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvent was distilled off
  8. 8
    Sonstigethe residue was purified by silica gel chromatography and recrystallization

Vorschrift

17.7 mL of 1N hydrochloric acid was added to Compound (7) dissolved in 17.7 mL of ethanol, followed by refluxing under heating for 2 hours. After cooling the reaction solution to ambient temperature, water was added to the solution. The aqueous layer was extracted with toluene, which was added to the organic layer, and the organic layer was washed with a saturated salt solution and then dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by silica gel chromatography and recrystallization to obtain 1.48 g of 1-(4-(4-(4-propylcyclohexyl)phenyl)-3-fluoro-2-hydroxyphenyl)-1-propanone (Compound (1-2-2-21)) as colorless crystals.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07740769B2uspto-grants-2010_06