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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1702Erstellt: 24. Oktober 2026

Carbon Dioxide → 2,2,2-Trifluoroethyl trifluoromethanesulfonate

https://huagongshe.com/de/reaction/1702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
Edukt2,2,2-TrifluoroethanolHCID 6409—
EduktTriethylamineHCID 8471—
EduktTrifluoromethanesulfonyl chlorideHCID 79000—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of trifluoromethanesulfonyl chloride (640 μL, 6 mmol) in CH2Cl2 (5 mL) was cooled under argon to -78° C. (IPA:dry ice bath). 2,2,2-Trifluoroethanol was added (365 μL, 5 mmol) and triethylamine (834 μL, 6 mmol) was added dropwise. The reaction was stirred for 1.5 hours then warmed to 0° C. for 1 hour. Anhydrous ether (20 mL) was added and the mixture was stirred at 0° C. for 30 minutes. The solids were filtered off and the solvent was removed under reduced pressure with the flask maintained at 0° C. This afforded the 2,2,2-trifluoroethyltriflate as a yellow oil which was used immediately.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05726172
Quelldatensatzuspto-grants-1998_03
ORD IDord-9773b48b03f44090887256b458e3e63d
Quellennotizuspto-grants-1998_03