HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → (1,1'-Biphenyl)-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | HCID 9855549 | HCID 9855549 | — |
| Reactant | Alumina | HCID 9989226 | — |
| Product | (1,1'-Biphenyl)-2-ol | HCID 7017 | — |
Reaction Steps
The same procedure as in Example 1 is repeated except that pellets of γ-alumina-calcium oxide (85:15 in weight ratio, baked product at 600° C for 3 hours) are used in place of the γ-alumina pellets. The conversion of the cyclohexanone dimer is confirmed to be always 100% during the 2,000 hours' reaction. Table 1 gives the selectivity for o-phenylphenol measured.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04060559 |
| Source dataset | uspto-grants-1977_11 |
| ORD ID | ord-f094710a411441a89bc5c4dd1035d47a |
| Source note | uspto-grants-1977_11 |