Home Chemistry Heterocyclic Building Blocks Piperidines 1-Isopropylpiperidine
Nucleophilic Substitution: The nitrogen atom in the piperidine ring can undergo nucleophilic substitution reactions with various electrophiles, leading to the formation of substituted piperidines.
Alkylation: The nitrogen atom in the piperidine ring can be alkylated by reaction with alkyl halides or sulfonates.
Acylation: The nitrogen atom in the piperidine ring can undergo acylation reactions to form N-acyl derivatives.
Reduction: The carbonyl group of the ketone can be reduced to the corresponding alcohols using reducing agents such as sodium borohydride or lithium aluminum hydride.
Oxidation: The alcohols group can be oxidized to the corresponding ketone or carboxylic acid under appropriate conditions.
Ring-opening Reactions: The piperidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Protonation: The nitrogen atom in the piperidine ring can be protonated under acidic conditions to form the corresponding ammonium salt.
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1-Isopropyl-piperidine-4-carboxaldehyde
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