Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2,5-Dioxopyrrolidin-1-Yl Benzoate
Hydrolysis: In the presence of water or an aqueous solution, the benzoate ester group may undergo hydrolysis to form benzoic acid and pyrrolidin-2,5-dione.
Base-Catalyzed Hydrolysis: The benzoate ester group may also undergo hydrolysis under basic conditions, leading to the formation of benzoic acid and pyrrolidin-2,5-dione.
Reaction with Nucleophiles: The carbonyl groups (C=O) present in the molecule can undergo nucleophilic addition reactions with nucleophiles. For instance, amines can react with the carbonyl group to form amides.
Decomposition at High Temperatures: The compound may undergo thermal decomposition at elevated temperatures, potentially leading to the formation of various products.
Reaction with Acids: The amide group (C(=O)NH-) in the pyrrolidin-2,5-dione moiety can react with strong acids to form the corresponding ammonium salt.
Oxidation: The compound may undergo oxidation under certain conditions, potentially leading to the formation of products with more oxygen-containing functional groups.
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2,5-Dioxopyrrolidin-1-yl 4-hydroxy-3,5-dimethylbenzoate
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2,5-Dioxopyrrolidin-1-yl 4-chlorobenzoate
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