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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50163생성일: 2026년 10월 23일

Sodium Hydroxide → 6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinoline

https://huagongshe.com/ko/reaction/50163

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
반응물6-Bromo4-(3-ethoxy-phenyl)-1h-quinolin-2-oneHCID 22465443—
용매1,1-DichloroethaneHCID 6365—
생성물6-Bromo4-(3-ethoxy-phenyl)-2-methoxy-quinolineHCID 2246541958.2%

반응 단계

To a suspension of 6-bromo-4-(3-ethoxy-phenyl)-1H-quinolin-2-one (7.4 g, 21.5 mmol) in 60 ml dichloroethane was added trimethyloxonium tetrafluoroborate (BF4OMe3, 3.66 g, 24.7 mmol). The resulting mixture was stirred at ambient temperature overnight. After cooling to 0° C., was added 60 ml of 10% aqueous NaOH dropwise. The reaction mixture was stirred for another six hours at ambient temperature. It was then partitioned between dichloromethane and water. The organic layer was washed brine, dried over MgSO4, filtered and concentrated under vacuum to give an off-white solid. The solid was chromatographed on flash silica gel eluting with dichoromethane to yield the titled compound of 23A as a white solid (4.48 g, 58% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710209B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-8cb0a23cb9cb4214a6753163d2276bc8
출처 메모uspto-grants-2004_03