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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281082Generated: October 31, 2026

Caprolactam → 6-Oxohexanoic acid

https://huagongshe.com/reaction/1281082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCaprolactamHCID 7768—
ReactantMethyl 6-oxohexanoateHCID 81164—
SolventWaterHCID 962—
Product6-Oxohexanoic acidHCID 440918—

Reaction Steps

A process for preparing ε-caprolactam is described in U.S. Pat. No. 4,730,040. In this process, methyl 5-formylvalerate is first hydrolyzed (step a) in the presence of water and an acidic agent to yield 5-formylvaleric acid. In this process, the 5-formylvaleric acid is reductively aminated in water through contact with ammonia and hydrogen using a ruthenium/zirconium on alumina catalyst, a Raney Nickel catalyst or a Raney Cobalt catalyst to obtain a 6-aminocaproic acid containing reaction mixture. After separation of ammonia, the reaction mixture obtained from the reductive amination is heated to 300° C. to form ε-caprolactam by cyclization of the 6-aminocaproic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06452002B2
Source datasetuspto-grants-2002_09
ORD IDord-7cb4340ed15c4f578086267a4bba5010
Source noteuspto-grants-2002_09