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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276840Generated: November 1, 2026

Benzyl Alcohol → Benzaldehyde

https://huagongshe.com/reaction/1276840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHydroquinoneHCID 785—
Reactant(Trifluoromethyl)benzeneHCID 7368—
ReactantPotassium CarbonateHCID 11430—
ProductBenzaldehydeHCID 240—
ProductBenzyl AlcoholHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166264
Source datasetuspto-grants-2000_12
ORD IDord-1ae7f5aaee2642589779883d6595d396
Source noteuspto-grants-2000_12