Sulfuric Acid → 8-Methoxy-3-methylquinoline

HRID 1167186

Reaktionsgleichung

Reaktionsgleichung von HRID 1167186
S(=O)(=O)(O)O.[CH3:6][O:7][C:8]1[C:9]([NH2:14])=[CH:10][CH:11]=[CH:12][CH:13]=1.O=[CH:16][C:17](=[CH2:19])[CH3:18].C(=O)([O-])[O-].[Na+].[Na+]>[I-].[Na+].O>[CH3:19][C:17]1[CH:16]=[N:14][C:9]2[C:10]([CH:18]=1)=[CH:11][CH:12]=[CH:13][C:8]=2[O:7][CH3:6]

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

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%)

Aufarbeitung

  1. customequipped with a mechanical stirrer
  2. additionthe dropwise addition
  3. temperatureThe mixture is then heated with an oil bath to 115° C.
  4. temperatureHeating
  5. additionafter the addition
  6. temperatureThe mixture is cooled to ambient temperature
  7. extractionExtraction
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. customevaporated under vacuum
  11. customThe residue is purified by silica gel chromatography (eluent: dichloromethane/methanol 98/2)

Quellen und Nachweise

ORD-Eintrag
ord-ca789576c5e543ae9d79d459a2376a0a
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06617336B1

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