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HRID 1645078作成日:2026年10月25日

N-methyl-3-(4-nitrophenoxy)benzamide → 3-(4-Aminophenoxy)-N-methylbenzamide

https://huagongshe.com/reaction/1645078

反応式

関与物質

役割名称HCID仕込み量
反応物N-methyl-3-(4-nitrophenoxy)benzamideHCID 23614569—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物3-(4-Aminophenoxy)-N-methylbenzamideHCID 2361457056.4%

反応手順

A slurry of 4-(3-(N-methylcarbamoyl)phenoxy)-1-nitrobenzene (1.89 g, 6.95 mmol) and 5% Pd/C (0.24 g) in EtOAc (20 mL) was stirred under an H2 atm (balloon) overnight. The resulting mixture was filtered through a pad of Celite® and concentrated under reduced pressure. The residue was purified by column chromatography (5% MeOH/95% CH2Cl2). The resulting oil solidified under vacuum overnight to give 4-(3-(N-methylcarbamoyl)phenoxy)aniline as a yellow solid (0.95 g, 56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124630B2
出典データセットuspto-grants-2012_02
ORD IDord-a7eda57b1a9044ba8c12c34b720cf494
出典メモuspto-grants-2012_02