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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363107Generated: November 1, 2026

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

https://huagongshe.com/reaction/363107

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 stirring 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 silica gel chromatography 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 numberUS05872137
Source datasetuspto-grants-1999_02
ORD IDord-09fe9937425340298731b24569419786
Source noteuspto-grants-1999_02