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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174443Generated: November 1, 2026

Hydrogen Peroxide → 4-Ethoxy-3-fluorophenol

https://huagongshe.com/reaction/1174443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
Reactant(4-Ethoxy-3-fluorophenyl)boronic acidHCID 2782821—
ReactantSodium BisulfiteHCID 23665763—
SolventTetrahydrofuranHCID 8028—
Product4-Ethoxy-3-fluorophenolHCID 18517276—

Reaction Steps

22.3 g of the crude 3-fluoro-4-ethoxyphenyl boronic acid obtained in the first step was dissolved in 200 ml of tetrahydrofuran, and 23.6 g (208 mmol) of aqueous 30% hydrogen peroxide was added while being kept at about 35° C. in a warm bath. After addition and after stirring the reaction solution at a room temperature for 24 hours, the reaction solution was poured into 300 ml of water, then sodium hydrogen sulfite was added and stirred at a room temperature for one hour. The reaction solution was extracted with 300 ml of ethyl acetate and the extracted layer was washed with water and then with an aqueous saturated sodium chloride solution successively and, after dying over anhydrous magnesium sulfate, concentrated under a reduced pressure. The concentrated residue was purified by silica gel column chromatography using a ethyl acetate/heptane mixed solvent as an eluent to obtain 17.6 g (113 mmol) of 3-fluoro-4-ethoxyphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838087B2
Source datasetuspto-grants-2010_11
ORD IDord-7b2a6723a3b44179ad8dfceb48c5df4a
Source noteuspto-grants-2010_11