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Trifluoroacetic acid → HCID 59398328, Verbindung

HRID 2193199
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2193199
FC(F)(F)C(O)=O.[O:8]1CCO[CH:9]1[CH2:13][N:14]1[C:23]2[C:18](=[C:19]([O:24][CH3:25])[CH:20]=[CH:21][CH:22]=2)[CH:17]=[CH:16][C:15]1=[O:26]>>[CH3:25][O:24][C:19]1[CH:20]=[CH:21][CH:22]=[C:23]2[C:18]=1[CH:17]=[CH:16][C:15](=[O:26])[N:14]2[CH2:13][CH:9]=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 6422Trifluoroacetic acidHCID 59397941HCID 59397941, Verbindung

Produkt 1

HCID 59398328HCID 59398328, Verbindung

Versuchsvorschrift

To 15 mL of 80% aqueous trifluoroacetic acid solution, 0.44 g of 1-(1,3-dioxolan-2-ylmethyl)-5-methoxyquinolin-2(1H)-one was added, and stirred at room temperature for 5 hours. The solvent was removed under reduced pressure, ethyl acetate and water were added, the organic layer was separated, and sodium chloride was added to the aqueous layer, and extracted twice with ethyl acetate. The organic layer and extracts were combined, washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure to give (5-methoxy-2-oxoquinolin-1(2H)-yl)acetaldehyde as a pale brown solid.

Aufarbeitung

  1. customThe solvent was removed under reduced pressure, ethyl acetate and water
  2. additionwere added
  • customthe organic layer was separated
  • additionsodium chloride was added to the aqueous layer
  • extractionextracted twice with ethyl acetate
  • washwashed with aqueous saturated sodium chloride solution
  • dry with materialdried over anhydrous magnesium sulfate
  • customthe solvent was removed under reduced pressure
  • Quellen und Nachweise

    ORD-Eintrag
    ord-705bc8cb6c21470e9505493403e6e59a
    Quelldatensatz
    uspto-grants-2012_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US08329694B2

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