Home Chemistry Heterocyclic Building Blocks Benzofurans Benzofuran-3(2H)-One
Hydrolysis: Benzofuran-3(2H)-one can undergo hydrolysis under basic or acidic conditions to form the corresponding carboxylic acid and an alcohols.
Reduction: The carbonyl group in benzofuran-3(2H)-one can be reduced to form a primary alcohol using reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: Benzofuran-3(2H)-one can be oxidized to form various compounds, depending on the reagent and conditions used. For instance, it can be oxidized to form a carboxylic acid or other derivatives.
Substitution Reactions: The aromatic ring in benzofuran-3(2H)-one can undergo electrophilic aromatic substitution reactions, where a substituent is added to the ring. This can be achieved with various electrophiles.
Condensation Reactions: Benzofuran-3(2H)-one can participate in condensation reactions with amines or other nucleophiles, leading to the formation of various products.
Cyclization Reactions: Depending on the conditions and reagents, benzofuran-3(2H)-one can participate in intramolecular cyclization reactions to form fused heterocycles or other cyclic compounds.
Photocycloaddition Reactions: Benzofuran-3(2H)-one may participate in photochemical reactions with suitable reactants to form new cyclic compounds.
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Methyl 2-(3-oxo-2,3-dihydrobenzofuran-6-yl)acetate
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