Reaktion #1909796
ord-99aefd1c7bb849d7b38987aea6b79e00
Reaktionsgleichung
1-[2-[4-(6-Methoxy-2-phenyl-3,4-dihydronaphthalen 1yl)phenoxy]ethyl]pyrrolidine hydrochloride
→
solid
Ausbeute 90.4%
cis-1-[2-[4-(6-methoxy-2-phenyl-1 ,2,3,4-tetrahydro-naphthalen-1yl)phenoxy]ethyl]pyrrolidine
Ausbeute 90.4%
Reagenzien
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigewas hydrogenated on a Parr shaker at 50° C.
- 2FiltrationThe catalyst was filtered off with the aid of Celite
- 3Sonstigethe solvents were removed in vacuo
- 4workup.DISSOLUTIONThe resulting white solid was dissolved in CH2Cl2
- 5Waschenthe solution was washed with saturated NaHCO3 (aq)
- 6TrocknenThe organic solution was dried (MgSO4)
- 7Filtrationfiltered
- 8Einengenconcentrated
Vorschrift
1-[2-[4-(6-Methoxy-2-phenyl-3,4-dihydronaphthalen 1yl)phenoxy]ethyl]pyrrolidine hydrochloride (nafoxidene hydrochloride) (75 g, 162 mmol) was dissolved in 1000 mL of EtOH and 300 mL of MeOH. Dry Pd(OH)2 on carbon was added and the mixture was hydrogenated on a Parr shaker at 50° C. and 50 psi (0.34 MPa) for 68 h. The catalyst was filtered off with the aid of Celite and the solvents were removed in vacuo. The resulting white solid was dissolved in CH2Cl2 and the solution was washed with saturated NaHCO3 (aq). The organic solution was dried (MgSO4), filtered, and concentrated to yield an off-white solid (62.6 g, 90%).