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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414957생성일: 2026년 10월 26일

2-Ethylcyclopentane-1,3-dione → 2-Ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dione

https://huagongshe.com/reaction/1414957

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethylcyclopentane-1,3-dioneHCID 69978—
반응물1-Diethylamino-6-(m-methoxyphenyl)-5-methylhexan-3-oneHCID 21485407—
반응물5-Methyl-6-(m-methoxyphenyl)hex-1-en-3-oneHCID 21485478—
용매Potassium HydroxideHCID 14797—
생성물2-Ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dioneHCID 21485626—

반응 단계

Add a mixture of 1-diethylamino-6-(m-methoxyphenyl)-5-methylhexan-3-one and 5-methyl-6-(m-methoxyphenyl)hex-1-en-3-one (6 g, prepared by slow distillation of the former substance) to 2-ethylcyclopentane-1,3-dione (3.5 g) in 0.12% methanolic potassium hydroxide (10 cc) and heat the mixture under reflux for 16 hours. Remove most of the solvent under reduced pressure and add ether (25 cc) and benzene (25 cc) to the residue. Wash the solution with 5% aqueous sodium hydroxide, water, dilute hydrochloric acid, and brine, and dry. Evaporate the solvent to obtain a viscous brown gum, which is the triketone 2-ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dione.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04002746
출처 데이터셋uspto-grants-1977_01
ORD IDord-f7f789b41872412795649383b740ece9
출처 메모uspto-grants-1977_01