Home Chemistry Heterocyclic Building Blocks Aromatic Heterocycles 3,4-Dihydronaphthalen-2(1H)-One
Aldol Condensation: Under basic conditions, 3,4-dihydronaphthalen-2(1H)-one can undergo aldol condensation reactions to form α,β-unsaturated ketones. This reaction involves the removal of a water molecule from two molecules of the compound.
Reduction: 3,4-dihydronaphthalen-2(1H)-one can be reduced to form a dihydronaphthalene derivative. Reduction can be achieved using various reducing agents such as sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Oxidation: The compound can undergo oxidation reactions to form naphthalene derivatives. Oxidizing agents like potassium permanganate (KMnO4) can be used for this purpose.
Substitution Reactions: Depending on the reaction conditions and reagents, 3,4-dihydronaphthalen-2(1H)-one can undergo various substitution reactions, including nucleophilic aromatic substitution (SNAr) reactions or electrophilic aromatic substitution (SEAr) reactions.
Ring-Opening Reactions: Under certain conditions, ring-opening reactions can occur to produce open-chain compounds.
Condensation Reactions: It can participate in condensation reactions with other compounds to form new products.
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7-Hydroxy-3,4-dihydro-1H-naphthalen-2-one
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7-Methoxy-1,1-dimethyl-3,4-dihydronaphthalen-2(1H)-one
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6-Fluoro-1-isopropyl-3,4-dihydronaphthalen-2(1H)-one
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8-Fluoro-3,4-dihydronaphthalen-2(1H)-one
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8-Bromo-3,4-dihydronaphthalen-2(1H)-one
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7,8-Difluoro-3,4-dihydronaphthalen-2(1H)-one
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7-Fluoro-3,4-dihydro-1H-naphthalen-2-one
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6-Methoxy-3,4-dihydronaphthalen-2(1H)-one
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6,7-Difluoro-3,4-dihydronaphthalen-2(1H)-one
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6,8-Dichloro-3,4-dihydronaphthalen-2(1H)-one
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6,7-Dichloro-3,4-dihydronaphthalen-2(1H)-one
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5,7-Dibromo-3,4-dihydronaphthalen-2(1H)-one
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5-Bromo-3,4-dihydronaphthalen-2(1H)-one
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5,6-Dichloro-3,4-dihydronaphthalen-2(1H)-one
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