Home Chemistry Organic Building Blocks Ketones Azepan-2-One
Polymerization: Caprolactam can undergo ring-opening polymerization to form nylon-6. In this process, caprolactam molecules are polymerized to create long chains of repeating units. This reaction typically involves the use of a catalyst and elevated temperature.
Hydrolysis: Caprolactam can be hydrolyzed to produce 6-aminohexanoic acid, which is a precursor to nylon-6. The hydrolysis reaction involves breaking the lactam ring, resulting in the formation of the carboxylic acid group.
Acylation: Caprolactam can be acylated by various acylating agents to introduce specific functional groups to the molecule. This reaction is often used to modify the caprolactam structure for specific applications.
Amidation: Caprolactam can be subjected to amidation reactions to form various amide derivatives by reacting with amines or other nucleophiles.
Oxidation: Caprolactam can be oxidized to produce various oxidation products, depending on the reaction conditions and reagents used.
Reduction: Caprolactam can be reduced to produce different amine derivatives, depending on the reagents and conditions employed.
Esterification: Caprolactam can undergo esterification reactions to form esters by reacting with carboxylic acids and appropriate catalysts.
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(S)-3-Amino-1-methylazepan-2-one hydrochloride
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(R)-tert-Butyl (2-oxoazepan-3-yl)carbamate
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(S)-tert-Butyl (2-oxoazepan-3-yl)carbamate
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