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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236073Generated: October 25, 2026

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

https://huagongshe.com/reaction/236073

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 liters of acetone is added a solution of 1.0 mole (110 g.) of hydroquinone in 1.1 liters 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 numberUS04642384
Source datasetuspto-grants-1987_02
ORD IDord-0c65e576f7e7433eacfd9b7e42b52547
Source noteuspto-grants-1987_02