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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604863생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/604863

반응식

참여 물질

역할이름HCID투입량
반응물1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 45480180—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 4548018178.3%

반응 단계

2520 mg (10.8 mmol) 1-(2-methoxy-4-nitro-phenyl)-4-methyl-1H-imidazole dissolved in ethanol (110 ml) was hydrated under an atmosphere of hydrogen at room temperature for 3½ hours in the presence of 252 mg of 10% palladium on charcoal. The catalyst was filtered off and washed with ethanol. The solvent of the filtrate was evaporated under reduced pressure. The crude product was purified on silica gel with methylene chloride/methanol 19/1. The fraction containing the product was suspended in diethyl ether, stirred for 15 minutes, filtered and dried to yield 1719 mg (78%) 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine as a yellow solid. MS ISP (m/e): 204.3 (100) (M+H)+. 1H NMR (CDCl3, 250 MHz): δ (ppm)=7.48 (s, 1H), 6.91 (d, 1H), 6.88 (s, 1H), 6.35 (s, 1H), 6.17 (d, 1H), 3.68 (s, 3H), 2.11 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910740B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-cdfdc24091ba44b497bd55592611929c
출처 메모uspto-grants-2011_03