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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7135생성일: 2026년 10월 24일

3-Bromoquinoline → 3-Methoxyquinoline

https://huagongshe.com/ko/reaction/7135

반응식

참여 물질

역할이름HCID투입량
반응물3-BromoquinolineHCID 21413—
반응물Sodium MethoxideHCID 10942334—
용매DimethylformamideHCID 6228—
생성물3-MethoxyquinolineHCID 5758076.2%

반응 조건

온도80 °C

반응 단계

A solution of 3-bromoquinoline (22.54 g, 108 mmol) in anhydrous DMF (110 mL) was treated with sodium methoxide (11.70 g, 217 mmol) and stirred at 80° C. for 16 hours. The reaction mixture was then concentrated and the residue taken up in ethyl acetate (300 mL) and water (60 mL). The organic phase was separated, washed with brine (2×60 mL), dried (MgSO4), filtered, concentrated and purified by column chromatography on silica gel (ethyl acetate/hexane; 1:3) to give 3-methoxyquinoline (1.06 g, 6%). 1H NMR (CDCl3) δ 3.95 (s, 3H), 7.38 (d, 1H, J=1.5 Hz), 7.54 (m, 2H), 7.72 (d, 1H, J=7.5 Hz), 8.04 (d, 1H, J=7.5 Hz), 8.67 (d, 1H, J=1.5 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084155B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-5203239c158e446e9e84abab6abb16bf
출처 메모uspto-grants-2006_08