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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47600생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물1-Cyclopentyloxy-2-methoxy-5-nitrobenzeneHCID 11390741—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물3-(Cyclopentyloxy)-4-methoxyanilineHCID 277933495.4%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699890B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-a78c2e88d66048de9707ae4a9542d381
출처 메모uspto-grants-2004_03