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HRID 475715作成日:2026年10月23日

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/ja/reaction/475715

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-methoxy-4-nitrophenyl)-3-methyl-1H-1,2,4-triazoleHCID 59577788—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)anilineHCID 5957781894.1%

反応手順

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, CDCl3) δ ppm 8.35 (s, 1H) 7.36 (d, J=8.55 Hz, 1H) 6.29-6.34 (m, 2H) 3.80 (s, 3H) 2.46 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637525B2
出典データセットuspto-grants-2014_01
ORD IDord-a23154dc9257412eae402184617fad35
出典メモuspto-grants-2014_01