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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206962Generated: November 1, 2026

Cyclohexanone Oxime → Laurolactam

https://huagongshe.com/reaction/2206962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanone OximeHCID 7517—
ReactantCaprolactamHCID 7768—
ReactantCyclododecanone, oximeHCID 136762—
ProductLaurolactamHCID 13690—

Reaction Steps

An oxime can be converted into an amide compound by Beckmann rearrangement reaction, particularly an oxime derived from a cyclic ketone can be converted into a lactam. For example, cyclohexanone oxime gives ε-caprolactam which is a starting material for Nylon 6 and cyclododecanone oxime gives laurolactam which is a starting material for Nylon 12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376375B2
Source datasetuspto-grants-2016_06
ORD IDord-ed521d42fbe74f65b2239ad9b8c43268
Source noteuspto-grants-2016_06