Home Chemistry Heterocyclic Building Blocks Piperidines 2-(Piperidin-4-Yl)Ethan-1-Ol
Oxidation: The primary alcohol group can be oxidized to an aldehyde and further to a carboxylic acid under stronger oxidizing conditions.
Esterification: It can undergo esterification reactions with carboxylic acids or acid chlorides to form esters.
Etherification: It can react with alkyl halides or alkyltosylates to form ethers.
Acetylation: It can be acetylated to form the corresponding acetate ester.
Nucleophilic substitution: The piperidine nitrogen can undergo nucleophilic substitution reactions with electrophiles.
Reduction: The carbonyl group of the aldehyde derivative obtained from oxidation can be reduced back to the alcohol, using reducing agents.
Ring-opening reactions: The piperidine ring can undergo ring-opening reactions under certain conditions, yielding various products depending on the reagents and conditions used.
Alkylation: The piperidine nitrogen can be alkylated by alkylhalides to form N-alkyl piperidine derivatives.
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2-(1-(3-Chloropropyl)piperidin-4-yl)ethanol
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