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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1874030생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1874030

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 번호US08304546B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-a5fcd6cafa3c4afd8240a21f97a07196
출처 메모uspto-grants-2012_11