Home Chemistry Heterocyclic Building Blocks Piperidines 1-Phenylpiperidin-2-One
Reduction: The ketone functionality in 1-phenylpiperidin-2-one can be reduced to yield 1-phenylpiperidine-2-one using reducing agents like sodium borohydride or lithium aluminum hydride.
Amination: The carbonyl group in 1-phenylpiperidin-2-one can be converted into an amine by reacting it with a suitable amine source (e.g., ammonia or an amine reagent), leading to the formation of an N-substituted piperidine derivative.
Acylation: 1-Phenylpiperidin-2-one can be acylated by reaction with acyl chlorides or anhydrides to introduce various acyl groups.
Grignard Reaction: The carbonyl group can be converted to an alcohol through a Grignard reaction with a suitable Grignard reagent, followed by acidification.
Condensation Reactions: 1-Phenylpiperidin-2-one can undergo various condensation reactions with different reagents to form cyclic or open-chain products, depending on the reaction conditions and reagents used.
Oxidation: The piperidine ring can be oxidized to the corresponding N-oxide or other oxidation products.
Ring-Opening Reactions: Under certain conditions, the piperidine ring can undergo ring-opening reactions, providing access to various functionalized products.
Cross-Coupling Reactions: The phenyl group in the compound can be functionalized using various cross-coupling reactions, such as Suzuki coupling, Stille coupling, or Heck reaction, to introduce different substituents.
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1-(2-Amino-6-methylphenyl)piperidin-2-one
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3,3-Dichloro-1-(4-nitrophenyl)piperidin-2-one
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3,3-Dichloro-1-(4-iodophenyl)piperidin-2-one
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