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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157912Generated: October 26, 2026

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

https://huagongshe.com/reaction/1157912

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 numberUS07807694B2
Source datasetuspto-grants-2010_10
ORD IDord-c86307b001514e55b4722bfe460549b5
Source noteuspto-grants-2010_10