Home Chemistry Heterocyclic Building Blocks Piperidines Piperidin-4-Ylmethanol
Oxidation: The hydroxyl group can be oxidized to form aldehydes, ketones, or carboxylic acids, depending on the conditions and reagents used.
Ether Formation: The hydroxyl group can undergo ether formation reactions with alkyl halides or alkyl sulfonates, leading to the formation of piperidin-4-ylmethyl ethers.
Esterification: The hydroxyl group can react with carboxylic acids or acid chlorides to form esters.
Amination: The hydroxyl group can undergo amination reactions to form secondary or tertiary amines.
Substitution Reactions: The piperidine ring can undergo substitution reactions at the nitrogen atom with various electrophiles, such as alkyl halides, acyl chlorides, or sulfonyl chlorides.
Reduction: The carbonyl group present in oxidized forms can be reduced back to the hydroxyl group using reducing agents.
Acetylation: The hydroxyl group can be acetylated to form acetates.
Ring Opening: Under specific conditions, the piperidine ring can undergo ring-opening reactions, leading to the formation of open-chain compounds.
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4-(Hydroxymethyl)piperidine-1-carbaldehyde
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Methyl 4-(hydroxymethyl)piperidine-1-carboxylate
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(4-Fluoropiperidin-4-yl)methanol hydrochloride
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(3,3-Difluoropiperidin-4-yl)methanol hydrochloride
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