Home Chemistry Heterocyclic Building Blocks Piperidines 2-(Piperidin-1-Yl)Ethan-1-Ol
Acetylation: The alcohol group can undergo acetylation, where an acetyl group (-COCH3) is added to form an acetate ester.
Oxidation: The alcohol group can be oxidized to form an aldehyde or a carboxylic acid, depending on the conditions and reagents used.
Ether Formation: The alcohol group can react with an alkyl halide in the presence of a base to form an ether.
Substitution Reaction: The piperidine ring can undergo substitution reactions at the nitrogen atom, for example, with alkyl halides to form N-alkylated piperidines.
Reduction: The carbonyl group of the piperidine ring could be reduced to form a secondary alcohol.
Esterification: The alcohol group can react with a carboxylic acid to form an ester.
Amidation: The alcohol group can react with an acid chloride or anhydrides to form an amide.
Ring Opening Reactions: The piperidine ring could undergo ring-opening reactions under certain conditions, leading to various products depending on the reagents and conditions used.
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2-(Piperidin-1-yl)ethan-1-ol hydrobromide
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1-(2-Hydroxyethyl)-2,2,6,6-tetramethylpiperidin-4-ol
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1-(2-Hydroxyethyl)piperidine-4-carbonitrile
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2-(5-Ethyl-2-methylpiperidin-1-yl)ethan-1-ol
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