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HCID 3106275, Verbindung → 3,5-Dinitropyridine

HRID 1416661
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1416661
[N+:1]([C:4]1[C:5](NN)=[N:6][CH:7]=[C:8]([N+:10]([O-:12])=[O:11])[CH:9]=1)([O-:3])=[O:2].C(O)=O.C=O>CO.C([O-])(=O)C.[Ag+]>[N+:10]([C:8]1[CH:7]=[N:6][CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:9]=1)([O-:12])=[O:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 3106275HCID 3106275, VerbindungHCID 18761834Formaldehyde formic acid

Produkt 1

HCID 5980543,5-DinitropyridineAusbeute 21,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 11246Silver acetateKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

Silver acetate (2.0 g) was added to a solution of the crude 3,5-dinitro-pyridinyl-hydrazine (2.2 g) in a mixture of methanol:H2O (1:1,6 ml), and the mixture was stirred at reflux overnight. Solvent was evaporated, then water and conc. NH4OH were added. The mixture was extracted with ethyl ether, the combined extracts were dried over MgSO4, concentrated and purified by column chromatography (5:1 hexane: ethyl acetate) to give the title compound (400 mg) in 21.8% yield. MS (DCI/NH3) m/e: 124 (M-46+1). 1H NMR (CDCl3, 300MHz) δ: 9.77 (m, 2H), 9.27 (m, 1H).

Aufarbeitung

  1. temperatureat reflux overnight
  2. customSolvent was evaporated
  3. additionwater and conc. NH4OH were added
  4. extractionThe mixture was extracted with ethyl ether
  5. dry with materialthe combined extracts were dried over MgSO4
  6. concentrationconcentrated
  7. custompurified by column chromatography (5:1 hexane: ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-6ff30fc9ce5c4ac4b557e3ed9a283134
Quelldatensatz
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05914328

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