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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167186Erstellt: 25. Oktober 2026

Sulfuric Acid → 8-Methoxy-3-methylquinoline

https://huagongshe.com/reaction/1167186

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktMethacroleinHCID 6562—
Edukt2-MethoxyanilineHCID 7000—
EduktSodium CarbonateHCID 10340—
KatalysatorSodium IodideHCID 5238—
LösungsmittelWaterHCID 962—
Produkt8-Methoxy-3-methylquinolineHCID 1398428629,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

94 ml of concentrated sulfuric acid and 70 ml of water are placed in a 1 l triple-necked flask equipped with a mechanical stirrer. The mixture is cooled to 0° C. with an ice bath and the dropwise addition is carried out of 45 g (366 mmol) of ortho-anisidine, followed by 0.54 g of sodium iodide. The mixture is then heated with an oil bath to 115° C. and 50 ml (604 mmol) of methacrolein are added using a syringe driver at the rate of 25 ml/h. Heating is continued for 1 h after the addition. The mixture is cooled to ambient temperature and then thrown onto a mixture of ice and of sodium carbonate. Extraction is carried out with dichloromethane. The organic phases are combined, dried over magnesium sulfate, filtered and evaporated under vacuum. The residue is purified by silica gel chromatography (eluent: dichloromethane/methanol 98/2) to provide 18.7 g of 3-methyl-8-methoxyquinoline. (Yield: 29.5%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617336B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-ca789576c5e543ae9d79d459a2376a0a
Quellennotizuspto-grants-2003_09