Home Chemistry Heterocyclic building blocks Piperidines Piperidin-2-ylmethanol
Oxidation: The hydroxymethyl group can be oxidized to form an aldehyde or carboxylic acid, depending on the conditions and reagents used.
Nucleophilic substitution: The hydroxymethyl group can undergo substitution reactions with suitable nucleophiles to form new compounds.
Acetylation: The hydroxyl group can be acetylated using acetic anhydrides or acetyl chloride to form the corresponding acetate ester.
Reduction: The carbonyl group of the piperidine ring can be reduced to form a secondary amine.
Ether formation: The hydroxyl group can undergo ether formation reactions with alkyl halides or alkyltosylates to form ethers.
Amination: The alcohol functionality can be converted into an amine through various methods, such as reductive amination or substitution.
Ring-opening reactions: The piperidine ring can undergo ring-opening reactions under specific conditions, yielding various products depending on the reagents and reaction conditions.
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tert-Butyl 2-(hydroxymethyl)piperidine-1-carboxylate
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(2S,4S)-tert-Butyl 4-amino-2-(hydroxymethyl)piperidine-1-carboxylate
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