Home Chemistry Heterocyclic Building Blocks Oxazolidines Oxazolidine-2,5-Dione
Nucleophilic Addition: The carbonyl groups in oxazolidine-2,5-dione can undergo nucleophilic addition reactions with various nucleophiles, such as amines, alcohols, and hydrazines.
Michael Addition: Oxazolidine-2,5-dione can participate in Michael addition reactions with nucleophiles containing an active hydrogen, such as thiols or amines. This can lead to the formation of a new carbon-carbon bond.
Oxidation: Oxazolidine-2,5-dione can be oxidized to produce various products depending on the reaction conditions and the oxidizing agent used.
Reduction: The carbonyl groups in oxazolidine-2,5-dione can be reduced to form the corresponding alcohol groups using reducing agents like sodium borohydride (NaBH4) or lithium aluminum hydride (LiAlH4).
Esterification: Oxazolidine-2,5-dione can react with alcohols in the presence of an acid catalyst to form esters.
Amidation: It can undergo amidation reactions with amines to produce amides.
Ring-Opening Reactions: Depending on the reaction conditions, oxazolidine-2,5-dione can undergo ring-opening reactions, leading to the formation of open-chain compounds.
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(S)-N-(4-(2,5-Dioxooxazolidin-4-yl)butyl)-2,2,2-trifluoroacetamide
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