HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Cyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Cumene | HCID 7406 | — |
| Reactant | Cyclohexylbenzene | HCID 13229 | — |
| Product | Cyclohexanone | HCID 7967 | — |
| Product | Cyclododecylbenzene | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06720462B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-b0fd436155b24925881a316335879af3 |
| Source note | uspto-grants-2004_04 |