Reaktion #309001

ord-996189ce869a4fd68f750cecc793eb69

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added dropwise via addition funnel
  2. 2
    Sonstigethe solvent was evaporated
  3. 3
    workup.STIRRINGThe residue was stirred in hexane/EtOAc
  4. 4
    Sonstigethe solid formed
  5. 5
    Filtrationwas filtered
  6. 6
    EinengenThe hexane/EtOAC solution was concentrated
  7. 7
    Sonstigepurified by ISCO graduate chromatography (hexane-20% EtOAc in hexane)

Vorschrift

A solution of triphenylphosphine (18.5 g, 70.6 mmol) and 40% DEAD in toluene (12.3 g, 70.6 mmol) in 125.0 mL of tetrahydrofuran was cooled to 0° C. under N2 as a solution of 1-(4-hydroxy-phenyl)-propan-2-one (6.54 g, 43.6 mmol) and 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (10.7 g, 53.2 mmol) in 125.0 mL of tetrahydrofuran was added dropwise via addition funnel. After stirred at rt overnight, the solvent was evaporated. The residue was stirred in hexane/EtOAc, the solid formed was filtered. The hexane/EtOAC solution was concentrated and purified by ISCO graduate chromatography (hexane-20% EtOAc in hexane) to give 4-[4-[2-oxo-propyl)-phenoxy]-piperidine-1-carboxylic acid tert-butyl ester (8.52 g, 59%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08207168B2uspto-grants-2012_06