Home Chemistry Organic Building Blocks Alkenyls Methylenecyclohexane
Hydrogenation: Methylenecyclohexane can undergo hydrogenation, a reaction in which hydrogen gas H2 is added to the double bond to form cyclohexylmethane. This is typically carried out in the presence of a catalyst, such as a metal catalyst (e.g., platinum, palladium, or nickel), to break the double bond.
Halogenation: Methylenecyclohexane can undergo halogenation reactions, where halogens such as chlorine or bromine add to the double bond to form the corresponding halogenated cyclohexane compounds.
Oxidation: Oxidation of methylenecyclohexane can lead to the formation of various oxidation products. For example, it can be oxidized to form cyclohexanone or cyclohexanol under appropriate conditions.
Isomerization: The alkylidene group in methylenecyclohexane can undergo isomerization reactions under certain conditions, leading to the formation of different isomers.
Cycloaddition Reactions: Methylenecyclohexane can participate in cycloaddition reactions, such as Diels-Alder reactions, with suitable dienophiles to form cycloadducts.
Ring-Opening Reactions: Under certain reaction conditions, the cyclohexane ring in methylenecyclohexane can undergo ring-opening reactions to form linear or branched compounds.
Substitution Reactions: The methylene group in methylenecyclohexane can undergo substitution reactions with appropriate reagents to replace the methylene group with other functional groups.
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Ethyl 4-methylenecyclohexanecarboxylate
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tert-Butyl (4-methylenecyclohexyl)carbamate
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