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HRID 723770作成日:2026年10月26日

Ammonium formate → 3-fluoro-4-(2-methyl-1H-imidazol-1-yl)aniline

https://huagongshe.com/reaction/723770

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium formateHCID 2723923—
反応物1-(2-fluoro-4-nitrophenyl)-2-methyl-1H-imidazoleHCID 21876645—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物3-fluoro-4-(2-methyl-1H-imidazol-1-yl)anilineHCID 21876620100.1%

反応手順

3-Fluoro-4-(2-methylimidazol-1-yl)nitrobenzene (40 g, 0.181 M) was dissolved in a mixture of methanol (200 ml) and tetrahydrofuran (800 ml), cooled to 0° under nitrogen, and treated with ammonium formate (57 g, 0.905 M) followed by palladium on charcoal (10%, 2 g). The mixture was stirred at ambient temperature for 18 hours, filtered through celite, celite washed with methanol (100 ml), and filtrate evaporated to dryness. The residue was partitioned between ethyl acetate (800 ml) and 10% aqueous sodium bicarbonate (250 ml). The organic layer was separated, washed with brine (250 ml), dried (magnesium sulfate) and evaporated to give title compound (34.6 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07141583B2
出典データセットuspto-grants-2006_11
ORD IDord-136172f2f8a74f21a1819ae17354115a
出典メモuspto-grants-2006_11