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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68138생성일: 2026년 10월 24일

3-Propoxynaphthalen-2-ylamine → 2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-one

https://huagongshe.com/ko/reaction/68138

반응식

참여 물질

역할이름HCID투입량
반응물3-Propoxynaphthalen-2-ylamineHCID 21279904—
반응물Ethyl alpha-(hydroxymethylene)-4-methoxyphenylacetateHCID 67418551—
용매BenzeneHCID 241—
생성물2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-oneHCID 4622439742.4%

반응 단계

To a benzene solution (50 ml) containing 3-propoxynaphthalen-2-ylamine (2.05 g, 10.18 mmol) and ethyl α-(hydroxymethylene)-4-methoxyphenylacetate (2.29 g, 10.3 mmol) was added 350 mg of Amberlyst 15 (Sigma-Aldrich). The resulting mixture was heated under reflux for 21 hours using a Dean-Stark trap. The reaction mixture was then cooled to room temperature, filtered to remove resin, and then the filtrate was concentrated under reduced pressure. Diphenyl ether (2.2 ml) was added to the residue, and the mixture was then heated with a mantle heater and stirred for 1.5 hours under reflux. The resulting reaction mixture was cooled to room temperature, and then directly purified using silica gel column chromatography (dichloromethane:methanol=100:1→60:1). The purified product was concentrated under reduced pressure to recrystallize the residue from ethyl acetate-n-hexane, giving a pale yellow powder of 2-(4-methoxyphenyl)-5-propoxy-4H-benzo[f]quinolin-1-one (1.55 g, yield: 42%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045108E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-2367e7ee6668415aa1e6575417a21c95
출처 메모uspto-grants-2014_09