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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1077140생성일: 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/1077140

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 6 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 번호US03959322
출처 데이터셋uspto-grants-1976_05
ORD IDord-7a35113cc7024972af5d9d45f8589e0a
출처 메모uspto-grants-1976_05