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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323688Generated: October 25, 2026

4-Benzyloxy-3-ethyl-5-methylphenyl benzoate → 2-Ethyl-6-methyl-4-benzoyloxyphenol

https://huagongshe.com/reaction/323688

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-3-ethyl-5-methylphenyl benzoateHCID 54236096—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-Ethyl-6-methyl-4-benzoyloxyphenolHCID 2328240995%

Reaction Steps

Then, 8.4 g of crude 4-benzyloxy-3-ethyl-5-methylphenyl benzoate was 5 dissolved in 100 ml of ethyl acetate, which was put into a reaction vessel, and the air in the vessel was replaced with nitrogen gas. Then, 0.5 g of 10% palladium on carbon was added, and the nitrogen gas in the vessel was replaced with hydrogen gas, followed by vigorous stirring at room temperature for 24 hours. The hydrogen gas in the vessel was replaced with nitrogen gas, after which the reaction mixture was filtered through cerite and the filtrate was concentrated under reduced pressure, which afforded 5.9 g of crude 3-ethyl-4-hydroxy-5-methylphenyl benzoate (95% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214835B1
Source datasetuspto-grants-2001_04
ORD IDord-45eeaeb8b8a34e5391c59ef01064f624
Source noteuspto-grants-2001_04