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HRID 451008생성일: 2026년 10월 24일

1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole → 3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline

https://huagongshe.com/ko/reaction/451008

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 45480180—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181100.6%

반응 단계

10% Palladium on carbon (250 mg) was added under an atmosphere of nitrogen to a chilled (ice-water bath) solution of 1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazole (2.56 g, 11.0 mmol) dissolved in methanol (150 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-(4-methyl-1H-imidazol-1-yl)aniline (2.25 g, 100% yield) as a blackish/grey waxy solid. LC-MS (M+H)+204.1. 1H NMR (500 MHz, CDCl3) δ ppm 7.69 (s, 1H) 7.01 (d, J=8.55 Hz, 1H) 6.82 (s, 1H) 6.33 (d, J=2.14 Hz, 1H) 6.30 (d, J=8.55 Hz, 1H) 3.78 (s, 3H) 2.33 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486952B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-29e8c83c3398439d84d12b34704aaaf7
출처 메모uspto-grants-2013_07