Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8968Generated: October 25, 2026

(4-(1H-Benzo[d]imidazol-2-yl)phenyl)methanol → 4-(1H-benzimidazol-2-yl)benzaldehyde

https://huagongshe.com/reaction/8968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(1H-Benzo[d]imidazol-2-yl)phenyl)methanolHCID 56965510—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-(1H-benzimidazol-2-yl)benzaldehydeHCID 2198517142%

Reaction Steps

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) δ 7.28 (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)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091217B2
Source datasetuspto-grants-2006_08
ORD IDord-952b8ed9281d4331b9d03bfc456f033a
Source noteuspto-grants-2006_08