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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1,4-Bis(2,2,2-trifluoroethoxy)benzene | HCID 737156 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04617396 |
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| Source dataset | uspto-grants-1986_10 |
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| ORD ID | ord-231a15f7b39a46d2a5140c3b641f6549 |
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| Source note | uspto-grants-1986_10 |
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