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Sodium Chloride → 5-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-one

HRID 272100
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 272100
[C:1]([C:4]1[CH:13]=[CH:12][C:11]([OH:14])=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:15])[NH:9]2)(=[O:3])[CH3:2].C(=O)([O-])[O-].[K+].[K+].[CH2:22](Br)[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.[Cl-].[Na+]>CN(C)C=O>[C:1]([C:4]1[CH:13]=[CH:12][C:11]([O:14][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[C:10]2[C:5]=1[CH:6]=[CH:7][C:8](=[O:15])[NH:9]2)(=[O:3])[CH3:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 5234Sodium ChlorideHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 119838955-Acetyl-8-hydroxy-2(1H)-quinolinone

Produkt 1

HCID 133754445-Acetyl-8-(benzyloxy)-1,2-dihydroquinolin-2-oneAusbeute 80,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To 5-acetyl-8-hydroxy-2-quinolone (37.7 g, 186 mmol) was added dimethylformamide (200 mL) and potassium carbonate (34.5 g, 250 mmol) followed by benzyl bromide (31.8 g, 186 mmol). The mixture was stirred at room temperature for 2.25 hour and then poured into saturated sodium chloride (3.5 L) at 0° C. and stirred well for 1 hour. The product was collected and dried on a Buchner funnel for 1 hour, and the resulting solids were dissolved in dichloromethane (2 L) and dried over sodium sulfate. The solution was filtered through a pad of Celite and washed with dichloromethane (5×200 mL). The combined filtrate was then concentrated to dryness and the resulting solids were triturated with ether (500 mL) for 2 hours. The product was collected on a Buchner funnel, washed with ether (2×250 mL) and dried under reduced pressure to give 5-acetyl-8-benzyloxy-2(1H)-quinolinone (EE) (44 g) as an off white powder.

Aufarbeitung

  1. stirringstirred well for 1 hour
  2. customThe product was collected
  3. customdried on a Buchner funnel for 1 hour
  4. dissolutionthe resulting solids were dissolved in dichloromethane (2 L)
  5. dry with materialdried over sodium sulfate
  6. filtrationThe solution was filtered through a pad of Celite
  7. washwashed with dichloromethane (5×200 mL)
  8. concentrationThe combined filtrate was then concentrated to dryness
  9. customthe resulting solids were triturated with ether (500 mL) for 2 hours
  10. customThe product was collected on a Buchner funnel
  11. washwashed with ether (2×250 mL)
  12. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-7c537465d0cc49ae9a96ff07c3f9bfde
Quelldatensatz
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07452995B2

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