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Potassium Carbonate → 2,5-Dichloropyridine-4-carbonitrile

HRID 637791
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 637791
O=P(Cl)(Cl)Cl.[Cl:6][C:7]1[CH:12]=[C:11]([CH:13]=[N:14]O)[C:10]([Cl:16])=[CH:9][N:8]=1.C([O-])([O-])=O.[K+].[K+]>C(#N)C>[Cl:6][C:7]1[CH:12]=[C:11]([C:13]#[N:14])[C:10]([Cl:16])=[CH:9][N:8]=1
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Komponenten

5

Edukt 3

HCID 11430Potassium CarbonateHCID 24813Phosphorus oxychlorideHCID 1363872824-Pyridinecarboxaldehyde, 2,5-dichloro-, oxime

Produkt 1

HCID 135602102,5-Dichloropyridine-4-carbonitrileAusbeute 77,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To 100 ml of acetonitrile was added 24.5 g of POCl3, followed by 27.1 g of 2,5-dichloro-4-pyridinecarboxaldehyde oxime (prepared as described in Example 4). The reaction mixture was heated at reflux temperature for 1 hour, then cooled and poured onto 300 g of ice. The pH of the mixture was adjusted to about pH 6 with K2CO3 and filtered. The filtrate was extracted with 100 ml of CH2Cl2. The filter cake and the CH2Cl2 solution were combined, diluted with equal volumes of hexane, treated with charcoal, dried, and concentrated. The residue was purified by distillation on a Kugelrohr distillation apparatus (boiling point 80° C. at 0.2 mm pressure) to give 19.0 g (77%) of the desired 2,5-dichloro-4-pyridinecarbonitrile as a white solid, m.p. 58°-60° C.

Aufarbeitung

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux temperature for 1 hour
  3. temperaturecooled
  4. filtrationfiltered
  5. extractionThe filtrate was extracted with 100 ml of CH2Cl2
  6. additiondiluted with equal volumes of hexane
  7. additiontreated with charcoal
  8. customdried
  9. concentrationconcentrated
  10. distillationThe residue was purified by distillation on a Kugelrohr distillation apparatus (boiling point 80° C. at 0.2 mm pressure)

Quellen und Nachweise

ORD-Eintrag
ord-ce726209030f425f86002d234f826cb2
Quelldatensatz
uspto-grants-1985_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04558134

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