Hydrochloric Acid → HCID 22624532, Verbindung

HRID 279162Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 279162
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[F:11][C:12]([F:30])([CH:27]([F:29])[F:28])[CH2:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([N:21]2[CH:25]=[N:24][NH:23][C:22]2=[O:26])=[CH:17][CH:16]=1.C(=O)([O-])[O-].[K+].[K+].Cl>C(OCC)(=O)C.O.CN(C)C=O>[N+:8]([C:5]1[CH:6]=[CH:7][C:2]([N:23]2[C:22](=[O:26])[N:21]([C:18]3[CH:17]=[CH:16][C:15]([O:14][CH2:13][C:12]([F:11])([F:30])[CH:27]([F:28])[F:29])=[CH:20][CH:19]=3)[CH:25]=[N:24]2)=[CH:3][CH:4]=1)([O-:10])=[O:9]

Komponenten

8

Edukt 4

HCID 313Hydrochloric AcidHCID 9590p-FluoronitrobenzeneHCID 11430Potassium CarbonateHCID 10779907HCID 10779907, Verbindung

Produkt 1

HCID 22624532HCID 22624532, VerbindungAusbeute 67 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

A mixture of 4-fluoronitrobenzene (3.1 g), 4-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-3(2H,4H)-1,2,4-triazolone (5.8 g), potassium carbonate (13.8 g) and N,N-dimethylformamide (60 ml) was stirred at 80° C. for 2 hours. The resultant was cooled and poured into water (500 ml). The mixture was neutralized with hydrochloric acid and the precipitated crystals were collected by filtration. The crystals thus obtained were dissolved in ethyl acetate (300 ml) and dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was crystallized from a mixture of ethyl acetate and diisopropyl ether to give 2-(4-nitrophenyl)-4-[4-(2,2,3,3-tetrafluoropropoxy)phenyl]-3(2H,4H)-1,2,4-triazolone (5.5 g, 67%) as yellow crystalline powders.

Aufarbeitung

  1. temperatureThe resultant was cooled
  2. filtrationthe precipitated crystals were collected by filtration
  3. customThe crystals thus obtained
  4. dry with materialdried over anhydrous magnesium sulfate
  5. filtrationAfter filtration
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customThe residue was crystallized from a mixture of ethyl acetate and diisopropyl ether

Quellen und Nachweise

ORD-Eintrag
ord-5e0b21859aac456284c4c3aaa8c06614
Quelldatensatz
uspto-grants-2002_03
Patentnummer
US06362206B1

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