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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285091Generated: October 30, 2026

Hydroquinone → 4-{[3-Fluoro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenol

https://huagongshe.com/reaction/1285091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant2,3-Difluoro-5-(trifluoromethyl)pyridineHCID 13421547—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-{[3-Fluoro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenolHCID 15592835—

Reaction Conditions

Temperature60 °C

Reaction Steps

Hydroquinone (4.4 g, 0.04 mole) was dissolved in 65 ml of dimethylsulfoxide and powdered sodium hydroxide (1.4 g, 0.035 mole) was added in one portion and the mixture stirred under nitrogen atmosphere for 10 minutes to convert to the sodium salt. 2,3-Difluoro-5-(trifluoromethyl)pyridine (6.0 g, 0.033 mole) was then added and the mixture stirred at 50° C. for 1.5 hours then warmed to 60° C. for a moment, let cool for 15 minutes and then poured into 500 ml of cold water. Additional sodium hydroxide (~3 g in water) was added to convert the desired product to its sodium salt. The insoluble bis-derivative was then removed by extraction with hexane. The clear aqueous phase was separated, cooled and acidified with concentrated hydrochloric acid. The solid which separated was collected on a filter, washed, dried on a vacuum funnel and taken up in hot hexane. After treating with decolorizing carbon, filtering, concentrating and cooling the white crystalline product separated. Yield: 2.6 g. M.P. 97.5-98.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565568
Source datasetuspto-grants-1986_01
ORD IDord-02fe0044261a4c9fa109baa2b59f9424
Source noteuspto-grants-1986_01