Reaktion #2315644

ord-57aa50f948cf4bfabfe8a0ce42a1839f

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschento elute
  2. 2
    Sonstigematerial (5.3 g), prepared as in Example 2
  3. 3
    workup.ADDITIONThe solution containing this enantiomer
  4. 4
    Einengenwas concentrated
  5. 5
    Sonstigea rotary evaporator

Vorschrift

R(−) N-(1,2,3,4-tetrahydro-1-naphthalenyl)homopiperazine was obtained as the second material to elute on subjecting racemic material (5.3 g), prepared as in Example 2, to preparative Chiral Pak AD HPLC resolution using a hexane/ethanol mixture with modification with diethylamine. The enantiomeric purity was determined on an analytical scale using hexane:ethanol:diethylamine (90:5:.05, v/v) and detection at 220 nm. The solution containing this enantiomer was concentrated using a rotary evaporator to give the title compound (2.65 g), [α]D22−94° (c=0.64, methanol); 98.5% ee.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06417183B1uspto-grants-2002_07