Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentylbenzene | HCID 10864 | — |
| Reactant | Perhydroxyl radical | HCID 18500 | — |
| Reactant | Cyclohexylbenzene hydroperoxide | HCID 86589629 | — |
| Product | Phenol | HCID 996 | — |
| Product | Cyclohexanone | HCID 7967 | — |
Reaction Steps
All cyclohexylbenzene hydroperoxide cleavage reactions were carried out in a 100 mL round bottom flask equipped with a magnetic stir bar. Generally, about 14 g of crude oxidation product (see Example I), 0.4 of internal standard (n-pentylbenzene), 0.1-3.0 g of catalyst and about 10 ml of solvent were charged to the vessel. The reactor contents were stirred at room temperature up to about 70° C. for 30 minutes to about 2 hours, then sampled for analysis by gas liquid chromatography (glc). The product yields are corrected for the fact that only 90% of the hydroperoxide in the CHBHP feed is the correct hydroperoxide, i.e. ##STR3## Other isomeric hydroperoxides are incapable of cleavage to give the desired ultimate products, phenol and cyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04480141 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-6131fb4f19894dee88da13e474ba9fd2 |
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| Source note | uspto-grants-1984_10 |
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