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HRID 1812098作成日:2026年10月25日

1-(2-Methoxyethoxy)-4-nitrobenzene → 4-(2-Methoxyethoxy)aniline

https://huagongshe.com/reaction/1812098

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-Methoxyethoxy)-4-nitrobenzeneHCID 547809—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物4-(2-Methoxyethoxy)anilineHCID 387988589.3%

反応手順

A mixture of 1-(2-methoxyethoxy)-4-nitrobenzene (0.724 g, 3.67 mmol) and 10% Pd/C (Aldrich) (0.201 g, 1.89 mmol) in EtOH (10 mL) was evacuated under vacuum and refilled with hydrogen (4 times). The mixture was hydrogenated under balloon pressure at rt for 1.5 h. The reaction mixture was filtered through a pad of Celite® (diatomaceous earth) (eluent:EtOH) and concentrated. The crude product was purified by silica gel chromatography (25 g, eluent: EtOAc in hexanes 0%-60%) to give 4-(2-methoxyethoxy)aniline (0.548 g, 89% yield) as a clear oil. 1H NMR (400 MHz, CDCl3) δ 6.73-6.82 (m, 2H); 6.58-6.68 (m, 2H); 4.01-4.08 (m, 2H); 3.67-3.76 (m, 2H); 3.29-3.52 (m, 5H). m/z (ESI, +ve ion) 168.1 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362241B2
出典データセットuspto-grants-2013_01
ORD IDord-1014bdbd1b734ba3bad3ae80323c48ca
出典メモuspto-grants-2013_01