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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1803124생성일: 2026년 10월 25일

1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole → 3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline

https://huagongshe.com/reaction/1803124

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazoleHCID 59577788—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)anilineHCID 5957781894.1%

반응 단계

Step F (2): 10% Palladium on carbon (1.2 g) was added under an atmosphere of nitrogen to a chilled (ice-water bath) solution of 1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazole (3.7 g, 12.7 mmol) dissolved in methanol (250 mL). The flask was repeated evacuated and flushed with hydrogen gas (double balloon). The resulting mixture was allowed to warm to rt and left to stir for 18 h under the hydrogen atmosphere. Purged with nitrogen gas. Filtered the crude reaction mixture through a short diatomaceous earth (Celite®) plug. Rinsed reaction vessel and plug with methanol. Concentrated filtrate in vacuo. Dried residue on high vacuum overnight to afford 3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline (2.44 g, 94% yield) as a reddish solid. LC-MS (M+H)+ 205.2. 1H NMR (500 MHz, chloroform-d) δ ppm 8.35 (s, 1 H) 7.36 (d, J=8.55 Hz, 1 H) 6.29-6.34 (m, 2 H) 3.80 (s, 3 H) 2.46 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08349880B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-568b323d659e48589de0d015cdd8d2db
출처 메모uspto-grants-2013_01