Reaktion #1669487

ord-094cb66795d547f282a1f69d89c89d68

Reaktionsgleichung

OCc1ccc(-c2nc3ccccc3[nH]2)cc1
4-(Benzimidazol-2-yl)-benzyl alcohol
O=Cc1ccc(-c2nc3ccccc3[nH]2)cc1
4-(benzimidazol-2-yl)-benzaldehyde
Ausbeute 42.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe mixture was filtered through celite
  2. 2
    Waschenthe cake washed with CH2Cl2
  3. 3
    Sonstigethe solvent from the eluent removed under reduced pressure

Vorschrift

4-(Benzimidazol-2-yl)-benzyl alcohol from above (0.175 g, 0.78 mmol) was dissolved in CH2Cl2 (5 mL) and THF (8 mL), treated with activated MnO2 (0.68 g, 7.8 mmol) and stirred at room temperature for 1.5 h. The mixture was filtered through celite, the cake washed with CH2Cl2 and the solvent from the eluent removed under reduced pressure to afford 4-(benzimidazol-2-yl)-benzaldehyde (92 mg, 42%). 1H NMR CD4OD) δ7.28 (m, 2H), 7.60 (br, 1H (NH)), 7.65 (d, 2H, J=7.8 Hz), 8.09 (d, 2H, J=7.8 Hz), 8.30 (d, 2H, J=9.0 Hz), 10.08 (s, 1H (CHO)).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06734191B2uspto-grants-2004_05