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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2299206생성일: 2026년 10월 26일

1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazole → 2-Fluoro-4-(1,2,4-triazol-1-yl)phenylamine

https://huagongshe.com/reaction/2299206

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-fluoro-4-nitrophenyl)-1H-1,2,4-triazoleHCID 21883919—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물2-Fluoro-4-(1,2,4-triazol-1-yl)phenylamineHCID 2188386664.1%

반응 단계

1-(3-Fluoro-4-nitrophenyl)-1H-1,2,4-triazole (3.06 g) was dissolved in ethanol (100 ml) and admixed with 10% Pd/C (50% water, 612 mg) and then stirred under a hydrogen atmosphere at room temperature for 1 hour. After filtering the catalyst off, the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate, and the resultant solution as washed successively with water and saturated brine, and 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=1:2). 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-(4-amino-3-fluorophenyl)-1H-1,2,4-triazole (1.68 g) as yellow powdery crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06495604B1
출처 데이터셋uspto-grants-2002_12
ORD IDord-b70b8a07105d416b8fe25803d4567585
출처 메모uspto-grants-2002_12