Home Chemistry Organic Building Blocks Ketones Cyclopent-2-En-1-One
Michael Addition: Cyclopent-2-en-1-one can undergo a Michael addition reaction with nucleophiles, such as amines or thiols, leading to the formation of a 1,5-dicarbonyl compound.
Enolization: Cyclopent-2-en-1-one can tautomerize to its enol form, which is an enediol. This enolization can participate in various reactions, including keto-enol tautomerism and reaction with electrophiles.
Reduction: It can undergo reduction reactions to form cyclopentanone using reducing agents like sodium borohydride (NaBH4).
Aldol Condensation: Cyclopent-2-en-1-one can participate in aldol condensation reactions with itself or other carbonyl compounds to form β-hydroxy ketones or α,β-unsaturated carbonyl compounds.
Wittig Reaction: It can react with a phosphonium ylide in a Wittig reaction to form alkenes.
Haloform Reaction: In the presence of halogen and base, it can undergo a haloform reaction, leading to the formation of haloform compounds.
Nucleophilic Addition: It can undergo nucleophilic addition reactions with various nucleophiles, such as amines, alcohols, and thiols, depending on the reaction conditions.
Oxidation: Cyclopent-2-en-1-one can be oxidized to form carboxylic acids using strong oxidizing agents.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Oxygen related+−
Formula Weight+−
click to sign in and save
3-Oxocyclopent-1-enecarboxylic acid
click to sign in and save
click to sign in and save
Methyl 3-oxocyclopent-1-enecarboxylate
click to sign in and save
2-Methyl-5-oxocyclopent-1-en-1-yl butyrate
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :