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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085612Generated: November 1, 2026

Acetone → Cyclohexanone

https://huagongshe.com/reaction/2085612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCumeneHCID 7406—
ReactantCyclohexylbenzeneHCID 13229—
ProductCyclohexanoneHCID 7967—
ProductCyclododecylbenzeneHCID 519199—

Reaction Steps

Both the preparation of the starting material prepared by alkylation, e.g. cumene, cyclohexylbenzene (in the Hock process, cyclohexylbenzene gives not acetone but cyclohexanone) and cyclododecylbenzene (in the Hock process, cyclododecylbenzene gives cyclododecanone), and the acid-catalysed cleavage and rearrangement to phenol which follow the oxidation step generally proceed with high selectivity to give high yields.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720462B2
Source datasetuspto-grants-2004_04
ORD IDord-b0fd436155b24925881a316335879af3
Source noteuspto-grants-2004_04