Home Chemistry Organic Building Blocks Ketones Morpholin-3-One
Nucleophilic Addition: Morpholin-3-one can react with nucleophiles, such as primary amines, to form imine derivatives or substituted morpholinones. The reaction is typically catalyzed by an acid.
Hydrolysis: Under acidic or basic conditions, the ketone functional group can undergo hydrolysis to form the corresponding carboxylic acid and morpholine.
Reduction: The carbonyl group of morpholin-3-one can be reduced to the corresponding alcohol (morpholin-3-ol) using reducing agents like sodium borohydride (NaBH4).
Ring Opening Reactions: The morpholine ring can be opened under various conditions. For example, treatment with strong acids can lead to ring opening and subsequent reactions with nucleophiles.
Condensation Reactions: It can participate in condensation reactions to form a variety of products. For example, it can react with carbonyl compounds in the presence of acid catalysts to form β-lactams or other related products.
Substitution Reactions: Depending on the reaction conditions and reagents, morpholin-3-one can undergo substitution reactions at various positions within the molecule.
Cyclization Reactions: Under certain conditions, morpholin-3-one can participate in intramolecular cyclization reactions to form bicyclic or spirocyclic compounds.
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tert-Butyl 3-oxomorpholine-4-carboxylate
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(R)-5-(Hydroxymethyl)-4-methylmorpholin-3-one
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