Home Chemistry Heterocyclic Building Blocks Morpholines 4-Phenylmorpholin-3-One
Hydrolysis: 4-Phenylmorpholin-3-one can undergo hydrolysis in the presence of an acid or base to form 4-phenylmorpholine and the corresponding acid or salt.
Reduction: It can be reduced to form 4-phenylmorpholine, typically using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Acylation: 4-Phenylmorpholin-3-one can be acylated by reacting it with acyl chlorides or anhydrides, leading to the introduction of acyl groups onto the morpholine ring.
Nucleophilic Substitution: The compound can undergo nucleophilic substitution reactions with various nucleophiles to modify the structure. For example, it can react with primary amines to form N-substituted derivatives.
Oxidation: It can be oxidized to produce various compounds, depending on the oxidizing agent used.
Ring Opening Reactions: 4-Phenylmorpholin-3-one contains a cyclic structure, and ring-opening reactions can be conducted with strong nucleophiles or bases.
Cyclization Reactions: Depending on the conditions and reagents, cyclization reactions can occur to form various cyclic compounds.
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