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Acetic Acid → 5(6H)-Quinolinone, 7,8-dihydro-

HRID 863009
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 863009
[NH2:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4](=[O:8])[CH:3]=1.C(O)(=O)C.[C:13]1(C)[CH:18]=CC=C[CH:14]=1>>[N:1]1[C:2]2[CH2:7][CH2:6][CH2:5][C:4](=[O:8])[C:3]=2[CH:18]=[CH:13][CH:14]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 176Acetic AcidHCID 1140TolueneHCID 788923-Aminocyclohex-2-en-1-one

Produkt 1

HCID 30168115(6H)-Quinolinone, 7,8-dihydro-

Versuchsvorschrift

A mixture of 57.93 g of 3-amino-2-cyclohexene-1-one, 76.8 g of 3-(dimethylamino)acrotein, 62.5 ml of glacial acetic acid and 270 ml of toluene is refluxed under argon for 16 hours and concentrated under vacuum to dryness. Toluene (200 ml) is added and the solvent removed under vacuum. To the residue is added one liter of dichloromethane and then 200 ml of saturated NaHCO3 slowly added and solid NaHCO3 added to bring the pH to 8. The mixture is filtered and the CH2Cl2 layer separated. The CH2Cl2 layer is passed through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness. The residual black oil is extracted with hot hexane and the hexane decanted. This process is repeated until no more product extracted into the hexane. The hexane extracts are combined and the solvent removed to give 17.3 g of product as an oil.

Aufarbeitung

  1. temperatureis refluxed under argon for 16 hours
  2. concentrationconcentrated under vacuum to dryness
  3. additionToluene (200 ml) is added
  4. customthe solvent removed under vacuum
  5. additionTo the residue is added one liter of dichloromethane
  6. addition200 ml of saturated NaHCO3 slowly added
  7. additionsolid NaHCO3 added
  8. filtrationThe mixture is filtered
  9. customthe CH2Cl2 layer separated
  10. concentrationthe filtrate concentrated to dryness
  11. extractionThe residual black oil is extracted with hot hexane
  12. customthe hexane decanted
  13. extractionextracted into the hexane
  14. customthe solvent removed

Quellen und Nachweise

ORD-Eintrag
ord-afdee911fb524958bdb6a268acf7272b
Quelldatensatz
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05719278

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