Reaktion #360046

ord-f80e5e9ad73a4aeb93feea1e5d49c8aa

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe mixture was stirred at 18-25° C. for 3.5 hours after which time LC analysis
  2. 2
    Sonstigethe reaction
  3. 3
    Filtrationthe resulting slurry filtered through a pad of aluminium oxide (activated, basic, Brockmann I, standard grade, ˜150 mesh) (481 g, 40 wt)
  4. 4
    Wascheneluting with 1% methanol/dichloromethane
  5. 5
    Sonstigeevaporated to dryness at 40° C
  6. 6
    workup.STIRRINGThe resulting brown solid was stirred in tertbutylmethylether (120 ml, 10 vol)
  7. 7
    SonstigeUndissolved residue was removed by filtration
  8. 8
    Waschenrinsed with tertbutylmethylether (3×120 ml, 3×10 vol)
  9. 9
    SonstigeThe combined filtrates were evaporated at 40° C.

Vorschrift

Pyridinium chlorochromate (20.3 g, 0.09415 mol), 1.69 wt) was charged to a stirred suspension of celite (24 g, 2 wt) and {4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-yl}methanol (12.03 g, 0.03766 mol) in dichloromethane (120 ml, 10 vol) with stirring. The mixture was stirred at 18-25° C. for 3.5 hours after which time LC analysis showed the reaction to be 70% complete. Magnesium sulphate (12 g, 1 wt) was added and the resulting slurry filtered through a pad of aluminium oxide (activated, basic, Brockmann I, standard grade, ˜150 mesh) (481 g, 40 wt) eluting with 1% methanol/dichloromethane. Clean fractions were combined and evaporated to dryness at 40° C. The resulting brown solid was stirred in tertbutylmethylether (120 ml, 10 vol). Undissolved residue was removed by filtration and rinsed with tertbutylmethylether (3×120 ml, 3×10 vol). The combined filtrates were evaporated at 40° C. to yield 4-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]tetrahydro-2H-pyran-4-carbaldehyde (6.0 g, 50.2%) as a beige waxy solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07456164B2uspto-grants-2008_11