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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788806Generated: November 4, 2026

Hydroquinone → 1,4-Bis(2,2,2-trifluoroethoxy)benzene

https://huagongshe.com/reaction/1788806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
SolventAcetoneHCID 180—
Product1,4-Bis(2,2,2-trifluoroethoxy)benzeneHCID 73715688%

Reaction Steps

To a mixture of 2.42 moles (334.4 g.) of potassium carbonate, 2.2 moles (510.6 g.) of 2,2,2-trifluoroethyl trifluoromethanesulfonate in 1.02 liter of acetone is added a solution of 1.0 mole (110 g.) of hydroquinone in 1.1 liter of acetone, slowly over a 2 hour period. The reaction is then heated at reflux for 24 hours, the reaction mixture is evaporated, and 2 liters of chloroform and 2 liters of water are added to the residue. The chloroform layer is separated, the aqueous layer is washed twice with 1 liter of chloroform, and the combined chloroform solution is washed with 1 liter of water. The chloroform solution is dried over magnesium sulfate, then concentrated under vacuum. Hexane is added to the residue and the solid product is collected by filtration and washed with hexane. Additional material is collected from the concentrated residues. A yield of 88 percent, 241 g. of 1,4-bis(2,2,2-trifluoroethoxy)benzene, m.p. 75°-77° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684733
Source datasetuspto-grants-1987_08
ORD IDord-2a80223beefe44d9b08f195aabbc7f3b
Source noteuspto-grants-1987_08