HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1702Erstellt: 24. Oktober 2026
Carbon Dioxide → 2,2,2-Trifluoroethyl trifluoromethanesulfonate
https://huagongshe.com/de/reaction/1702
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Trifluoromethanesulfonyl chloride | HCID 79000 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Isopropanol | HCID 3776 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05726172 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-9773b48b03f44090887256b458e3e63d |
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| Quellennotiz | uspto-grants-1998_03 |
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