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HRID 47600作成日:2026年10月24日

1-Cyclopentyloxy-2-methoxy-5-nitrobenzene → 3-(Cyclopentyloxy)-4-methoxyaniline

https://huagongshe.com/ja/reaction/47600

反応式

関与物質

役割名称HCID仕込み量
反応物1-Cyclopentyloxy-2-methoxy-5-nitrobenzeneHCID 11390741—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物3-(Cyclopentyloxy)-4-methoxyanilineHCID 277933495.4%

反応手順

To a suspension of 10% Pd on activated carbon (25 g) in ethanol (4L), under N2 protection, was added 1-cyclopentyloxy-2-methoxy-5-nitrobenzene (250 g, 1.054 mol). The reaction mixture was degassed under vacuum three times. The reaction mixture was stirred vigorously while hydrogen gas was allowed to flow over the reaction mixture. After 4 h the reaction was complete by TLC (5:1 hex:EA). The reaction mixture was filtered through a pad of celite and the celite was rinsed with additional ethanol. The solvent was removed in-vacuo to obtain 208.38 g (95% yield) of 3-cyclopentyloxy-4-methoxyaniline as a red liquid. 1H NMR (CDCl3) δ 6.85 (d. J=8.4 Hz, 1H), 6.29 (s, 1H), 6.19 (dd, J=2.8, 8.4, 1H), 4.69 (p, J=4.4 Hz, 1H), 3.75 (s, 3H), 3.44 (bs, 2H),1.90-1.81 (m, 6H), 1.61-1.55 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06699890B2
出典データセットuspto-grants-2004_03
ORD IDord-a78c2e88d66048de9707ae4a9542d381
出典メモuspto-grants-2004_03