Home Chemistry Organic Building Blocks Aliphatic Cyclic Hydrocarbons Naphthalene-1,4-Dione
Reduction: Naphthalene-1,4-dione can be reduced to yield naphthalene-1,4-dihydroquinone. This reduction can be achieved using reducing agents like sodium borohydride (NaBH4) or other suitable reducing agents.
Oxidation: Naphthalene-1,4-dione can be further oxidized to produce various oxidative products. For instance, it can be converted into various quinone derivatives or undergo side-chain oxidation reactions.
Substitution Reactions: Naphthalene-1,4-dione can undergo electrophilic aromatic substitution reactions. Various substituents can be added to the naphthalene ring system.
Michael Addition: Naphthalene-1,4-dione can participate in Michael addition reactions with nucleophiles, typically enolate or enamine intermediates.
Cycloaddition Reactions: It can also participate in cycloaddition reactions, such as Diels-Alder reactions, with suitable diene or dienophile partners.
Acylation: Naphthalene-1,4-dione can be acylated to introduce acyl groups onto the naphthalene ring.
Condensation Reactions: It can be involved in condensation reactions with amines or other nucleophiles to form various condensed compounds.
Polymerization: In some cases, naphthalene-1,4-dione can be used as a building block in the synthesis of polymers and resins.
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2-Chloro-3-(2-methoxyethylamino)naphthalene-1,4-dione
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2,3-Dichloro-5,8-dihydroxynaphthalene-1,4-dione
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