Home Chemistry Heterocyclic Building Blocks Piperidines Phenyl(Piperidin-1-Yl)Methanone
Reduction: Phenyl(piperidin-1-yl)methanone may undergo reduction reactions to form secondary amines or other reduced derivatives. Common reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4) might be used.
Acylation: It may undergo acylation reactions, where an acyl group is introduced. This can occur with reagents like acyl chlorides or anhydrides in the presence of a suitable base or catalyst.
Nucleophilic Substitution: If there are appropriate leaving groups, nucleophiles may substitute them. For example, if there's a halogen on the molecule, it could be substituted by a nucleophile in the presence of a base.
Oxidation: Depending on the conditions, it could potentially undergo oxidation reactions. This could lead to the formation of various oxidation products.
Hofmann Rearrangement: This is a specific type of rearrangement reaction for primary amides. It can be induced by treatment with chlorine or bromine in the presence of a strong base.
Grignard Reaction: Phenyl(piperidin-1-yl)methanone could potentially react with a Grignard reagent, forming a new carbon-carbon bond.
Cyclization: Given its structural features, it may undergo intramolecular cyclization reactions under specific conditions.
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(3-Aminophenyl)(2-(2-hydroxyethyl)piperidin-1-yl)methanone
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(3-(3-(Ethoxycarbonyl)piperidine-1-carbonyl)phenyl)boronic acid
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(3-Bromo-5-fluorophenyl)(piperidin-1-yl)methanone
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(3-Bromo-5-chlorophenyl)(piperidin-1-yl)methanone
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4-(Piperidine-1-carbonyl)phenylboronic acid
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3-(Piperidine-1-carbonyl)phenylboronic acid
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(4-(Aminomethyl)piperidin-1-yl)(phenyl)methanone hydrochloride
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(2,6-Dimethylpiperidin-1-yl)(2-fluoro-4-methylphenyl)methanone
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1-(2-Fluorobenzoyl)piperidine-4-carboxylic acid
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1-(2-Chlorobenzoyl)piperidine-4-carboxylic acid
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1-[4-(Trifluoromethyl)benzoyl]piperidine-4-carboxylic acid
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(3-(4-Methylpiperidine-1-carbonyl)phenyl)boronic acid
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(4-Chloro-3-(piperidine-1-carbonyl)phenyl)boronic acid
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(3-Chloro-5-(piperidine-1-carbonyl)phenyl)boronic acid
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