Home Chemistry Organic Building Blocks Ketones 1,3-Diphenylpropan-1-One
Aldol Condensation: 1,3-Diphenylpropan-1-one can undergo aldol condensation reactions to form α,β-unsaturated ketones. In the presence of a base, such as sodium hydroxide (NaOH) or sodium ethoxide (NaOEt), it can react with another molecule of itself or with other carbonyl compounds.
Michael Addition: Chalcones can undergo Michael addition reactions with nucleophiles such as amines, thiols, or enolates. This reaction leads to the formation of new carbon-carbon bonds.
Benzoin Condensation: Under appropriate conditions, chalcones can undergo benzoin condensation to yield α,α'-dihydroxy ketones.
Halogenation: The α,β-unsaturated carbonyl group in chalcones can be halogenated, typically using reagents like bromine or chlorine.
Nucleophilic Addition: Chalcones can react with various nucleophiles to form addition products. For example, they can react with hydrazine to form hydrazones.
Cyclization: Chalcones can undergo intramolecular cyclization reactions to form cyclic compounds under specific reaction conditions.
Cross-Coupling Reactions: Chalcones can participate in cross-coupling reactions with various coupling partners in the presence of appropriate catalysts. For example, Suzuki-Miyaura or Heck coupling reactions.
Enolate Chemistry: Like other ketones, chalcones can undergo enolization reactions, leading to the formation of enol or enolate intermediates. These can react with electrophiles to form new carbon-carbon bonds.
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3-(3,4-Dimethoxyphenyl)-1-(3-hydroxyphenyl)propan-1-one
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3-(4-Methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one
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