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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387248Generated: October 31, 2026

4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene → 4-Benzoyloxy-2-chloro-6-methylphenol

https://huagongshe.com/reaction/1387248

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzeneHCID 18504554—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthyl AcetateHCID 8857—
Product4-Benzoyloxy-2-chloro-6-methylphenolHCID 1850458896%

Reaction Steps

A reaction vessel was charged with 35 g of 4-benzyloxy-3-chloro-5-methyl-1-benzoyloxybenzene and 200 ml of ethyl acetate, and the air in the vessel was replaced with nitrogen. Then, 2 g of 10% palladium carbon was added, and the nitrogen in the vessel was replaced with hydrogen, followed by vigorous stilling at room temperature for 10 hours. The hydrogen in the vessel was replaced with nitrogen, after which the reaction mixture was filtered, and the filtrate was concentrated. The residue was subjected to silica gel chromatography, which afforded 25 g of 4-benzoyloxy-2-chloro-6-methylphenol (96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268313B1
Source datasetuspto-grants-2001_07
ORD IDord-0560c4a8cad5451baef8755fc9b89b91
Source noteuspto-grants-2001_07