Home Chemistry Heterocyclic Building Blocks Pyrrolidines 1-(Pyrrolidin-1-Yl)Ethan-1-One
Nucleophilic Addition: The carbonyl group can undergo nucleophilic addition reactions with nucleophiles such as Grignard reagents, organolithium compounds, or hydride donors.
Substitution Reactions: The carbon atom adjacent to the carbonyl group can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Condensation Reactions: It can participate in condensation reactions to form cyclic compounds or larger molecules.
Reduction: The carbonyl group can be reduced to form the corresponding alcohol using reducing agents like lithium aluminum hydride or sodium borohydride.
Acylation: The nitrogen atom in the pyrrolidine ring can undergo acylation reactions to form N-acyl derivatives.
Ring-closing Reactions: The compound may undergo intramolecular cyclization reactions to form cyclic compounds.
Oxidation: The carbonyl group can be oxidized to form carboxylic acid derivatives.
Hydrolysis: Under acidic or basic conditions, the compound can undergo hydrolysis to cleave the carbonyl group and form corresponding carboxylic acids or their derivatives.
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(R)-tert-Butyl (1-acetylpyrrolidin-3-yl)carbamate
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