Chemistry Organic Building Blocks Aryls 2-phenylnaphthalene
Ambeed provide 12 derivatives of 2-phenylnaphthalene.
These compounds have the same murcko framework: 2-phenylnaphthalene.
Electrophilic Aromatic Substitution (EAS): Like other aromatic compounds, 2-phenylnaphthalene can undergo EAS reactions. In these reactions, an electrophile (an electron-deficient species) substitutes for a hydrogen atom on the aromatic ring. Common EAS reactions include nitration, halogenation, sulfonation, and Friedel-Crafts acylation/alkylation.
Reduction: 2-Phenylnaphthalene can be reduced to form 2-phenylnaphthalene or even fully saturated compounds (tetrahydronaphthalene) using reducing agents like hydrogen gas H2 and a catalyst or using chemical reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: Oxidation of 2-phenylnaphthalene can lead to the formation of various oxidation products. For instance, mild oxidation using reagents like chromic acid (H2CrO4) or potassium permanganate (KMnO4) can lead to the formation of carboxylic acids. Stronger oxidizing agents may lead to further oxidation to ketones or other functional groups.
Hydrogenation: Under appropriate conditions, hydrogenation reactions can convert 2-phenylnaphthalene into 2-phenylnaphthalene or even fully saturated compounds.
Grignard Reaction: 2-Phenylnaphthalene can undergo Grignard reactions with appropriate Grignard reagents, leading to the formation of new carbon-carbon bonds.
Rearrangement Reactions: Depending on the reaction conditions and reagents, 2-phenylnaphthalene may undergo rearrangement reactions, leading to different isomeric products.
Photochemical Reactions: Ultraviolet (UV) or visible light exposure can lead to photochemical reactions in aromatic compounds like 2-phenylnaphthalene. These reactions may result in the formation of photoproducts, such as isomers or radicals.
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4-(6-(Methoxycarbonyl)naphthalen-2-yl)benzoic acid