HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → Benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | (Trifluoromethyl)benzene | HCID 7368 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Product | Benzaldehyde | HCID 240 | — |
| Product | Benzyl Alcohol | HCID 244 | — |
Reaction Steps
To a mixture of 0.1 millimole of Ru(PPh3)3Cl2 [dichlorotris(triphenylphosphine)ruthenium(II)], 0.1 millimole of hydroquinone, 0.03 millimole of potassium carbonate and 6 ml of trifluoromethylbenzene was added 1 millimole of benzyl alcohol, and the resultant mixture was stirred under oxygen atmosphere (1 atm) at 50° C. for 15 hours. The products were subjected to chromatography on silica gel (eluent: hexane/ethyl acetate=10/1) for the isolation to give benzaldehyde in a conversion rate of benzyl alcohol of 80% (yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166264 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-1ae7f5aaee2642589779883d6595d396 |
| Source note | uspto-grants-2000_12 |