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Phosphorus oxychloride → 2-Chloro-5-methyl-3-nitropyridine

HRID 1943748
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1943748
[CH3:1][C:2]1[CH:3]=[C:4]([N+:9]([O-:11])=[O:10])[C:5](O)=[N:6][CH:7]=1.P(Cl)(Cl)([Cl:14])=O>[Cl-].C([N+](C)(C)C)C1C=CC=CC=1.C(#N)C>[Cl:14][C:5]1[C:4]([N+:9]([O-:11])=[O:10])=[CH:3][C:2]([CH3:1])=[CH:7][N:6]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 178430719HCID 178430719, Verbindung

Produkt 1

HCID 8183002-Chloro-5-methyl-3-nitropyridineAusbeute 97 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 5963Benzyltrimethylammonium chlorideKatalysatorHCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

5-methyl-3-nitro-pyridin-2-ol (5 g, 32.4 mmol) and benzyltrimethyl ammonium chloride (3.01 g, 16.2 mmol) were dissolved in acetonitrile, and phosphorus oxychloride (9.0 ml, 97.2 mmol) was added thereto and stirred at 800 for 6 hours. The reaction mixture was cooled and poured into ice water to quench the reaction, and extracted with dichloromethane. The combined organic layer was washed with saturated saline solution, dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure. The residue was purified by column chromatography on silica eluting with a solvent of dichloromethane. The fractions containing the product were collected and evaporated to obtain 2-chloro-5-methyl-3-nitro-pyridine as yellow solid (5.39 g, 97%).

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. customto quench
  3. customthe reaction
  4. extractionextracted with dichloromethane
  5. washThe combined organic layer was washed with saturated saline solution
  6. dry with materialdried over anhydrous sodium sulfate (Na2SO4)
  7. filtrationfiltered
  8. customevaporated under reduced pressure
  9. customThe residue was purified by column chromatography on silica eluting with a solvent of dichloromethane
  10. additionThe fractions containing the product
  11. customwere collected
  12. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-c2ff4a311979427c82e72970c4596d9b
Quelldatensatz
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08394792B2

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