Home Chemistry Heterocyclic Building Blocks Imidazolidines Imidazolidin-2-One
Reductive Amination: Imidazolidin-2-one can react with primary amines and reducing agents (such as sodium cyanoborohydride or sodium borohydride) to form secondary amines. This reaction is a common method for introducing an amino group.
Oxidation: Imidazolidin-2-one can be oxidized using oxidizing agents like potassium permanganate (KMnO4) or hydrogen peroxide (H2O2) to form the corresponding oxo compound, which may further undergo reactions like ring opening or addition.
Ring Opening: The imidazolidin-2-one ring can be opened under various conditions, including the use of strong bases, acids, or nucleophiles. This leads to the formation of products with a variety of functional groups.
Nucleophilic Addition: Imidazolidin-2-one can undergo nucleophilic addition reactions with a variety of nucleophiles, such as amines, thiols, and Grignard reagents, depending on the specific conditions.
Condensation Reactions: Imidazolidin-2-one can be involved in condensation reactions to form larger cyclic or acyclic compounds. For example, it can react with carbonyl compounds to form various heterocyclic compounds.
Redox Reactions: Depending on the reaction conditions and reagents, imidazolidin-2-one can be involved in redox reactions, leading to the formation of products with different oxidation states.
Alkylation and Acylation: Imidazolidin-2-one can be alkylated or acylated using appropriate alkyl or acyl halides in the presence of a base to introduce alkyl or acyl groups onto the ring.
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(S)-tert-Butyl 1-methyl-2-oxoimidazolidine-4-carboxylate
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(R)-2-Oxoimidazolidine-4-carboxylic acid
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(S)-1-methyl-2-oxoimidazolidine-4-carboxylic acid
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