HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390361Generated: October 26, 2026
quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanol → quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanone
https://huagongshe.com/reaction/390361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanol | HCID 59419662 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanone | HCID 59419663 | — |
Reaction Steps
A mixture of quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanol, (Intermediate 12) 3.7 g, 7.9 mmol) in CH2Cl2 (50 mL) was treated with manganese(IV) oxide, activated (commercially available from Aldrich): MnO2 (4.1 g, 47.4 mmol) at room temperature. The mixture was heated to 60° C. for 2 h. The mixture was then cooled to room temperature and filtered through celite and the solvent was removed under vacuum to get quinolin-8-yl(1-trityl-1H-imidazol-5-yl)methanone, (Intermediate 13) (3.6 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383646B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-665549a522b14cc78a45c5c1ccbe8dd0 |
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| Source note | uspto-grants-2013_02 |
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