cyclohexanecarboxylic acid-Aliphatic Cyclic Hydrocarbons| Ambeed

: Alkylation: The piperidine nitrogen can be alkylated using alkyl halides or alkyl sulfonates to form N-alkylated derivatives. Amination: The azetidine nitrogen can undergo amination reactions, where it is converted into a new amine derivative. This can be achieved using various amine sources and appropriate reaction conditions. Ring Opening: The azetidine ring can be opened under specific reaction conditions, leading to the formation of new compounds. This may involve the use of strong acids or bases. Substitution Reactions: Other substitution reactions can occur at various positions of the molecule, depending on the reagents and reaction conditions. Reduction: The molecule can be reduced to form a saturated piperidine derivative. This can be achieved using reducing agents such as lithium aluminum hydride (LiAlH₄) or hydrogen gas in the presence of a catalyst. Oxidation: Oxidation reactions can modify the molecule by introducing oxygen-containing functional groups. This can be achieved using various oxidizing agents. Cyclization: Depending on the reaction conditions and reagents used, the compound may undergo intramolecular cyclization reactions to form cyclic derivatives. Hydrolysis: The compound can undergo hydrolysis reactions in the presence of acids or bases, leading to the cleavage of certain bonds and the formation of hydrolyzed products.