Cyclohexanone oxime is an organic compound containing the functional group oxime. This colorless solid is an important intermediate in the production of nylon 6, a widely used polymer.

Cyclohexanone oxime can be prepared from the condensation reaction between cyclohexanone and hydroxylamine:

Alternatively, another industrial route involves the reaction of cyclohexane with nitrosyl chloride, which is a free radical reaction. This method is advantageous as cyclohexane is much cheaper than cyclohexanone.

The most famous and commercially important reaction of cyclohexanone oxime is its Beckmann rearrangement yielding ε-caprolactam:

This reaction is catalyzed by sulfuric acid, but industrial scale reactions use solid acids.

Typical of oximes, the compound can be reduced by sodium amalgam gives cyclohexylamine. It can also be hydrolyzed with acetic acid to give back cyclohexanone.

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