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HRID 604863作成日:2026年10月26日

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

https://huagongshe.com/reaction/604863

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-methoxy-4-nitrophenyl)-4-methyl-1H-imidazoleHCID 45480180—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 4548018178.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910740B2
出典データセットuspto-grants-2011_03
ORD IDord-cdfdc24091ba44b497bd55592611929c
出典メモuspto-grants-2011_03