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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429706생성일: 2026년 10월 24일

Ethyl Bromide → 9-((N-(5-hydroxypentyl)-N-(ethyl)amino)methyl)anthracene

https://huagongshe.com/ko/reaction/429706

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물Potassium CarbonateHCID 11430—
반응물9-((5-Hydroxypentyl)aminomethyl)anthraceneHCID 10880907—
용매AcetonitrileHCID 6342—
생성물9-((N-(5-hydroxypentyl)-N-(ethyl)amino)methyl)anthraceneHCID 2266220198%

반응 단계

9-((5-hydroxypentyl)aminomethyl)anthracene (1.00 g, 3.41 mol) and K2CO3 (0.518 g, 3.75 mmol) were taken up in 25 mL acetonitrile. Ethyl bromide (11.14 g, 102 mmol) was added and the mixture was refluxed under nitrogen for 24 h. The mixture was filtered on a sintered-glass frit and the solvent and excess ethyl bromide was removed under reduced pressure. Removal of the solvent afforded 1.07 g (98% yield) of 6 as a yellow solid; 1H NMR (300.13 MHz, CD3CN) δ1.15 (m, 2H), 1.38 (m, 5H), 1.81 (m, 2H), 3.05 (m, 4H), 3.49 (t, 2H), 5.21 (s, 2H), 7.45 (m, 2H), 7.62 (m, 2H), 8.05 (d, 2H), 8.44 (m, 3H); 13C-{1H} NMR (75.4 MHz, CDCl3) δ131.8, 131.3, 130.8, 129.6, 128.0, 125.6, 124.0, 61.7, 53.1, 49.4, 48.7, 31.4, 23.9, 23.3, 10.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06319540B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-83dd505ddd544a2fa1374a4e5e365c3b
출처 메모uspto-grants-2001_11