Home Chemistry Heterocyclic Building Blocks Piperidines 2-(Piperidin-2-Yl)Ethan-1-Ol
Acetylation: The hydroxy group can be acetylated to form the corresponding acetate ester.
Oxidation: The alcohol group can be oxidized to form the corresponding aldehyde or carboxylic acid depending on the conditions and reagents used.
Alkylation: The piperidine nitrogen can undergo alkylation reactions with alkyl halides or alkylating agents.
Ether formation: The alcohol group can undergo ether formation reactions with alkyl halides or alkoxide ions.
Substitution reactions: The piperidine ring can undergo nucleophilic substitution reactions at the ring carbon atoms or at the nitrogen atom.
Reduction: The compound can be reduced to the corresponding amine using reducing agents such as lithium aluminum hydride or hydrogen in the presence of a catalyst.
Esterification: The compound can react with carboxylic acids in the presence of acid catalysts to form esters.
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(R)-2-(Piperidin-2-yl)ethanol hydrochloride
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(S)-2-(2-Hydroxyethyl)piperidine hydrochloride
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tert-Butyl 2-(2-hydroxyethyl)piperidine-1-carboxylate
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