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HRID 1414957Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1414957

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Ethylcyclopentane-1,3-dioneHCID 69978—
Edukt1-Diethylamino-6-(m-methoxyphenyl)-5-methylhexan-3-oneHCID 21485407—
Edukt5-Methyl-6-(m-methoxyphenyl)hex-1-en-3-oneHCID 21485478—
LösungsmittelPotassium HydroxideHCID 14797—
Produkt2-Ethyl-2-(6-m-methoxyphenyl-5-methyl-3-oxohexyl)cyclopentane-1,3-dioneHCID 21485626—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04002746
Quelldatensatzuspto-grants-1977_01
ORD IDord-f7f789b41872412795649383b740ece9
Quellennotizuspto-grants-1977_01