Home Chemistry Organic Building Blocks Ketones Cyclopentane-1,3-Dione
Aldol Condensation: Cyclopentane-1,3-dione can undergo aldol condensation reactions with itself or other carbonyl compounds, leading to the formation of β-hydroxyketones. This reaction involves the nucleophilic addition of one carbonyl group to the other, followed by dehydration.
Keto-Enol Tautomerism: Like other carbonyl compounds, cyclopentane-1,3-dione can exist in a keto-enol tautomeric equilibrium. In the enol form, one of the carbonyl groups becomes a hydroxyl group (-OH). This tautomeric shift is catalyzed by both acid and base.
Reduction: The ketone groups in cyclopentane-1,3-dione can be reduced to the corresponding alcohol groups using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Oxidation: Cyclopentane-1,3-dione can be oxidized to produce various compounds. Oxidation can convert the ketone groups into carboxylic acids or other oxidized derivatives.
Ring Closure: Under certain conditions, cyclopentane-1,3-dione can undergo ring-closure reactions to form cyclic compounds with different ring sizes.
Reactions with Grignard Reagents: Grignard reagents can add to the carbonyl groups in cyclopentane-1,3-dione, resulting in the formation of new carbon-carbon bonds.
Metal-Catalyzed Reactions: Transition metal catalysts can be used to promote various reactions, such as hydrogenation, oxidation, and cross-coupling reactions.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Oxygen related+−
Formula Weight+−
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :