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HRID 2299205Erstellt: 24. Oktober 2026

1H-1,2,4-Triazole → 1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazole

https://huagongshe.com/de/reaction/2299205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-1,2,4-TriazoleHCID 9257—
EduktPotassium CarbonateHCID 11430—
Edukt2,4-DifluoronitrobenzeneHCID 67967—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazoleHCID 2188391950,6%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

2,4-Difluoronitrobenzene (8.0 g) was dissolved in N,N-dimethylformamide (110 ml) and the solution was admixed with 1H-1,2,4-triazole (3.47 g) and potassium carbonate (6.95 g) and the mixture was stirred under a nitrogen atmosphere at 70° C. for 20 hours. The reaction mixture was diluted with ethyl acetate and washed with water. The aqueous layer was extracted with ethyl acetate, and the ethyl acetate layers were combined and washed 5 times with water and then with saturated brine, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate/hexane=1:1.3). A desired fraction was concentrated under reduced pressure and the residue was crystallized from a mixture of ethyl acetate and diisopropyl ether to yield 1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazole (5.29 g) as yellow powdery crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06495604B1
Quelldatensatzuspto-grants-2002_12
ORD IDord-ecb7d74152ca42e6b877fbad88b73f12
Quellennotizuspto-grants-2002_12