HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Propylphenol → 4-Propylcyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Propylphenol | HCID 12580 | — |
| Reactant | 4-Propylcyclohexanone | HCID 142482 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Propylcyclohexanol | HCID 2775094 | — |
Reaction Steps
In addition, the 4-propylcyclohexanone employed as a raw material in this preparation example was prepared as follows: A commercial p-n-propylphenol was hydrogenated in the presence of ethanol, sodium ethoxide and Raney nickel catalyst, under a hydrogen pressure of 100 atm, at 150° C. to form 4-n-propylcyclohexanol, which was then oxidized with Jones reagent (CrO3 /H2SO4 /H2O) in acetone to obtain 4-n-propylcyclohexanone having a b.p. of 110°~113° C./26 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04211666 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-45510c2c41bc4e43beb9d27e9af245af |
| Source note | uspto-grants-1980_07 |