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Phosphorus oxychloride → 2-Chloro-6,7-dimethylquinoline-3-carbonitrile

HRID 2413151
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2413151
[C:1]([C:3]1[C:4](=O)[NH:5][C:6]2[C:11]([CH:12]=1)=[CH:10][C:9]([CH3:13])=[C:8]([CH3:14])[CH:7]=2)#[N:2].P(Cl)(Cl)([Cl:18])=O>>[Cl:18][C:4]1[C:3]([C:1]#[N:2])=[CH:12][C:11]2[C:6](=[CH:7][C:8]([CH3:14])=[C:9]([CH3:13])[CH:10]=2)[N:5]=1
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Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 133714281,2-Dihydro-6,7-dimethyl-2-oxo-3-quinolinecarbonitrile

Produkt 1

HCID 133714332-Chloro-6,7-dimethylquinoline-3-carbonitrile

Versuchsvorschrift

A mixture was prepared from 67.5 g of 3-cyano-6,7-dimethyl-2(1H)-quinolinone and 340 ml of phosphoryl chloride and this was heated at reflux for 18 hours. The mixture was cooled, excess phosphoryl chloride was removed by vacuum evaporation, and the residue was carefully added to water with vigorous stirring. The solid which formed was separated by filtration and recrystallized from methylene chloride to give 2-chloro-3-cyano-6,7-dimethylquinoline melting at about 189°-190° C.

Aufarbeitung

  1. temperaturethis was heated
  2. temperatureat reflux for 18 hours
  3. temperature
The mixture was cooled
  • customexcess phosphoryl chloride was removed by vacuum evaporation
  • additionthe residue was carefully added to water with vigorous stirring
  • customThe solid which formed
  • customwas separated by filtration
  • customrecrystallized from methylene chloride
  • Quellen und Nachweise

    ORD-Eintrag
    ord-0d595101550b4d03b90c8c286d071b75
    Quelldatensatz
    uspto-grants-1985_01
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US04496569

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