Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161372Generated: October 28, 2026

Hydrogen Peroxide → 2-Fluoro-5-methoxyphenol

https://huagongshe.com/reaction/1161372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrimethyl borateHCID 8470—
Reactant4-FluoroanisoleHCID 9987—
ReactantPentamethyldiethylenetriamineHCID 18196—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-methoxyphenolHCID 14118957—

Reaction Steps

To a 200 ml THF solution containing 50.1 g of 1-fluoro-4-methoxybenzene and 70 g of N,N,N′,N′,N″-pentamethyldiethylenetriamine there was added dropwise 150 ml of n-butyllithium (2.66 M, hexane solution) over a period of 30 minutes, at −74° C. under a nitrogen atmosphere. After stirring for 3 hours at between −74° C. and −70° C., 100 ml of trimethyl borate was added. The temperature of the reaction mixture was then slowly allowed to rise to room temperature. Next, 70 ml of acetic acid and 75 ml of 30% aqueous hydrogen peroxide were added, and the reaction mixture was stirred overnight at room temperature. Water was then added to the reaction mixture, and then it was extracted with a mixture of hexane and ethyl acetate and dried over anhydrous magnesium sulfate. The desiccating agent was filtered off, and the filtrate was concentrated under reduced pressure to give a crude product of 1-fluoro-2-hydroxy-4-methoxybenzene (65.59 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816522B2
Source datasetuspto-grants-2010_10
ORD IDord-ffc72892b9d84e258167541a9c0795d9
Source noteuspto-grants-2010_10