HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → 4-Pentylphenyl 4-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | 4-Pentylphenyl 4-(benzyloxy)benzoate | HCID 13810576 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Pentylphenyl 4-hydroxybenzoate | HCID 13660589 | 93.2% |
Reaction Steps
To 100 mL of dehydrated ethanol, 15.6 g (41.5 mmol) of 4-benzyloxy-benzoic acid 4-pentyl-phenyl ester, 25 mL of cyclohexene, and 0.78 g of palladium hydroxide/carbon were added. Then, the mixture was refluxed for 10 hours under argon. The resulting reaction mixture was filtered, and the filtered liquid was concentrated. The residue was recrystallized from toluene. As a result, 11.0 g of a white solid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07758932B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-cd5adff26bbe4a9fbbcacec78848cc75 |
| Source note | uspto-grants-2010_07 |