Home Chemistry Heterocyclic Building Blocks Dioxolanes 2-Phenyl-1,3-Dioxolane
Ring Opening Reactions: The dioxolane ring can undergo ring-opening reactions under certain conditions. Common reagents for ring opening include acids, bases, and nucleophiles. Depending on the reaction conditions and the reagents used, you can obtain various products.
Substitution Reactions: The phenyl group on the molecule is susceptible to various substitution reactions, including electrophilic aromatic substitution (EAS) reactions. For example, you can introduce different functional groups onto the phenyl ring through reactions like Friedel-Crafts acylation or alkylation.
Oxidation and Reduction: The compound can be oxidized or reduced depending on the reaction conditions. For example, you can reduce the carbonyl group within the dioxolane ring to form a diol or oxidize it to form a diketone.
Grignard Reactions: The compound can undergo Grignard reactions, which involve the formation of a Grignard reagent (RMgX) and subsequent addition to the carbonyl group to form an alcohol.
Hydrolysis: The dioxolane ring can be hydrolyzed under acidic or basic conditions to yield different products, including diols or carboxylic acids.
Esterification: The compound can undergo esterification reactions with appropriate reagents to form ester derivatives.
Reductive Amination: If the carbonyl group is reduced to an alcohol, you can perform reductive amination reactions by reacting the alcohol with an amine to form an amine-containing compound.
Halogenation: You can halogenate the phenyl ring or the dioxolane ring using appropriate halogenating agents.
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2-Ethoxy-4-(4-methyl-1,3-dioxolan-2-yl)phenol
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2-Methoxy-4-(4-methyl-1,3-dioxolan-2-yl)phenol
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Benzaldehyde Propylene Glycol Acetal
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