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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290633Generated: October 30, 2026

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

https://huagongshe.com/reaction/2290633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroquinoneHCID 785—
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 carbonates, 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 numberUS04617396
Source datasetuspto-grants-1986_10
ORD IDord-231a15f7b39a46d2a5140c3b641f6549
Source noteuspto-grants-1986_10