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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2299205생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2299205

반응식

참여 물질

역할이름HCID투입량
반응물1H-1,2,4-TriazoleHCID 9257—
반응물Potassium CarbonateHCID 11430—
반응물2,4-DifluoronitrobenzeneHCID 67967—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazoleHCID 2188391950.6%

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06495604B1
출처 데이터셋uspto-grants-2002_12
ORD IDord-ecb7d74152ca42e6b877fbad88b73f12
출처 메모uspto-grants-2002_12