HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-(1H-Benzo[d]imidazol-2-yl)phenyl)methanol → 4-(1H-benzimidazol-2-yl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-(1H-Benzo[d]imidazol-2-yl)phenyl)methanol | HCID 56965510 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1H-benzimidazol-2-yl)benzaldehyde | HCID 21985171 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091217B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-952b8ed9281d4331b9d03bfc456f033a |
| Source note | uspto-grants-2006_08 |