Reaktion #2315644
ord-57aa50f948cf4bfabfe8a0ce42a1839f
Reaktionsgleichung
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Waschento elute
- 2Sonstigematerial (5.3 g), prepared as in Example 2
- 3workup.ADDITIONThe solution containing this enantiomer
- 4Einengenwas concentrated
- 5Sonstigea 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.