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Phosphorus oxychloride → 4-Chloro-5,7-dimethoxyquinoline

HRID 1013710
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1013710
[CH3:1][O:2][C:3]1[CH:12]=[C:11]([O:13][CH3:14])[CH:10]=[C:9]2[C:4]=1[C:5](O)=[CH:6][CH:7]=[N:8]2.O=P(Cl)(Cl)[Cl:18]>C1(C)C=CC=CC=1>[Cl:18][C:5]1[C:4]2[C:9](=[CH:10][C:11]([O:13][CH3:14])=[CH:12][C:3]=2[O:2][CH3:1])[N:8]=[CH:7][CH:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178493398HCID 178493398, Verbindung

Produkt 1

HCID 178804724-Chloro-5,7-dimethoxyquinoline

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

To a mixture of crude 5,7-dimethoxyquinolin-4-ol (5.36 g, 26 mmol) and Hunig'sBase (9.1 ml, 52 mmol) in toluene, was added POCl3(29 ml, 313 mmol). The mixture was refluxed for 5 h. Excess POCl3 was removed under reduced pressure and azeotroped with toluene. The resultant gum was treated with sat. NaHCO3 until no gas generated. The mixture was extracted with EtOAc, the organic extracts were combined and washed with sodium bicarbonate and solvent removed under reduced pressure. The crude product was purified via column chromatography on silica gel (RediSep 120 g column, gradient elution with 0-50% EtOAc/DCM) to afford 4-chloro-5,7-dimethoxyquinoline as a yellow solid. MS Found m/z=[M+H]+. 224.2 Calc'd for C11H10ClN: 223.7.

Aufarbeitung

  1. temperatureThe mixture was refluxed for 5 h
  2. customExcess POCl3 was removed under reduced pressure
  3. customazeotroped with toluene
  4. additionThe resultant gum was treated with sat. NaHCO3 until no gas
  5. extractionThe mixture was extracted with EtOAc
  6. washwashed with sodium bicarbonate and solvent
  7. customremoved under reduced pressure
  8. customThe crude product was purified via column chromatography on silica gel (RediSep 120 g column, gradient elution with 0-50% EtOAc/DCM)

Quellen und Nachweise

ORD-Eintrag
ord-da56e637f03248c59a005a2723f3670a
Quelldatensatz
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07981891B2

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