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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 578602Erstellt: 27. Oktober 2026

Benzo(h)quinoline → 5H-Indeno(1,2-b)pyridin-5-one

https://huagongshe.com/reaction/578602

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzo(h)quinolineHCID 9191—
EduktPotassium HydroxideHCID 14797—
EduktPotassium PermanganateHCID 516875—
LösungsmittelWaterHCID 962—
Produkt5H-Indeno(1,2-b)pyridin-5-oneHCID 7748942%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09040174B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-b82aa90264c945b48071577e904f9c19
Quellennotizuspto-grants-2015_05