Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 236073Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/236073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydroquinoneHCID 785—
EduktPotassium CarbonateHCID 11430—
Edukt2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—
LösungsmittelAcetoneHCID 180—
Produkt1,4-Bis(2,2,2-trifluoroethoxy)benzeneHCID 73715688%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04642384
Quelldatensatzuspto-grants-1987_02
ORD IDord-0c65e576f7e7433eacfd9b7e42b52547
Quellennotizuspto-grants-1987_02