HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 623390Erstellt: 24. Oktober 2026
2-Methyl-8-hydroxyquinoline → 8-Hydroxy-2-quinolinecarboxaldehyde
https://huagongshe.com/de/reaction/623390
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Methyl-8-hydroxyquinoline | HCID 13224 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 8-Hydroxy-2-quinolinecarboxaldehyde | HCID 599342 | 38% |
Reaktionsschritte
A solution of 8-hydroxy-2-methylquinoline (6.0 g, 37.7 mmol) in dioxane (15 ml) was added to a stirred solution of SeO2 (6.3 g, 56.8 mmol) in dioxane (80 ml) dropwise at 50° C. and the mixture was heated up to 80° C. for further 20 h. The resulting mixture was filtered. The filtrate was concentrated and the residue purified by column chromatography with Hex/EA=(15:1 to 10:1) to give 8-hydroxyquinoline-2-carboxaldehyde (2.45 g, 38%) derivatives as intermediates. Intermediate was converted into N-substituted compounds by reductive amination with aminoalcohol, aminoalkyne or other heterocycles to give series of compounds. 8-alkoxy-2-methyl quinoline were oxidized to give 8-alkoxyquinoline-2-carboxaldehyde derivatives and followed by the same method to give compounds M to O.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09302992B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-8ccab9494bbe4804b713961b03c5e461 |
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| Quellennotiz | uspto-grants-2016_04 |
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