HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzo(h)quinoline → 5H-Indeno(1,2-b)pyridin-5-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzo(h)quinoline | HCID 9191 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | Potassium Permanganate | HCID 516875 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5H-Indeno(1,2-b)pyridin-5-one | HCID 77489 | 42% |
Reaktionsschritte
A solution of benzo[h]quinoline (6 g, 33.5 mmol) and KOH (5.6 g, 100.5 mmol) in water (400 mL) was boiled. A hot solution of KMnO4 (14.8 g, 93.8 mmol) in water (240 mL) was added dropwise over 1 hour to the boiling solution. The mixture was refluxed for another 6 hours and filtered hot. The filtrate was allowed to cool to room temperature. The organic layer was extracted with chloroform and water, dried with anhydrous magnesium sulfate. After solvent removal, the residue was purified by column chromatography on silica (acetone-petroleum ether) to give product 2.5 g (42%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09040174B2 |
| Quelldatensatz | uspto-grants-2015_05 |
| ORD ID | ord-b82aa90264c945b48071577e904f9c19 |
| Quellennotiz | uspto-grants-2015_05 |