Home Chemistry Organic Building Blocks Ketones Cyclohex-2-En-1-One
Michael Addition: Cyclohex-2-en-1-one can undergo a Michael addition reaction with nucleophiles such as amines, thiols, and enolates.
Aldol Condensation: In the presence of a base, cyclohex-2-en-1-one can undergo an aldol condensation reaction with another carbonyl compound to form a β-hydroxy ketone or a β-diketone.
Benzoin Condensation: In the presence of a suitable catalyst (e.g., cyanide ions), cyclohex-2-en-1-one can undergo a benzoin condensation reaction with aldehydes to form α,α'-dihydroxyketones.
Ring-Opening Reactions: Under certain conditions, cyclohex-2-en-1-one can undergo ring-opening reactions to form open-chain compounds.
Alkylation: Cyclohex-2-en-1-one can be alkylated at the carbonyl oxygen using alkylating agents in the presence of a Lewis acid catalyst.
Halogenation: The double bond in cyclohex-2-en-1-one can be halogenated (e.g., bromination or chlorination) under appropriate conditions.
Enamine Formation: Cyclohex-2-en-1-one can form an enamine when reacted with a secondary amine in the presence of an acid catalyst.
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Ethyl 2-methyl-6-oxocyclohex-1-ene-1-carboxylate
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2-Hydroxy-3,5,5-trimethyl-2-cyclohexen-1-one
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Methyl 2,6-dimethyl-4-oxocyclohex-2-enecarboxylate
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Ethyl 2,6-dimethyl-4-oxocyclohex-2-enecarboxylate
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Ethyl 2-methyl-4-oxocyclohex-2-enecarboxylate
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