Reaktion #1743779

Reaktionsgleichung

N-2-(4-Nitrophenoxy)ethyl-4-(4-nitrophenoxy)piperidine

→

N-2-(4-aminophenoxy)ethyl-4-(4-aminophenoxy)piperidine

Ausbeute 80.0%

Lösungsmittel

THF MeOH

Reaktionsbedingungen

Aufarbeitung

1. 1
   FiltrationThe mixture was filtered through solka floc
2. 2
   Einengenthe filtrate was concentrated
3. 3
   SonstigePurification by flash chromatography (8% MeOH/CHCl3)

Vorschrift

N-2-(4-Nitrophenoxy)ethyl-4-(4-nitrophenoxy)piperidine (1.50 g, 3.87 mmol) was hydrogenated in THF/MeOH (1:1, 60 mL) at 50 psi over 10% Pd/C (0.5 g) for 16 hours. The mixture was filtered through solka floc and the filtrate was concentrated. Purification by flash chromatography (8% MeOH/CHCl3) gave 0.97 g (80%) of N-2-(4-aminophenoxy)ethyl-4-(4-aminophenoxy)piperidine as a yellow oil. 1H NMR (DMSO-d6): δ 6.65 (d, 4H), 6.50 (d, 4H), 4.60 (br s, 4H), 4.05 (m, 1H), 3.90 (t, 2H), 2.78 (m, 2H), 2.60 (t, 2H), 2.15 (m, 2H), 1.85 (m, 2H), 1.55 (m, 2H).

Quelle