HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trifluoroethanol → 2,2,2-Trifluoroethyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Product | 2,2,2-Trifluoroethyl trifluoromethanesulfonate | HCID 80366 | 73% |
Reaction Steps
In a 100-ml flask equipped with a stirrer, a thermometer, a nitrogen introducing pipe and a condenser, 50 ml (0.297 mol) of trifluoromethanesulfonic anhydride and 25 ml (0.342 mole) of 2,2,2-trifluoroethanol were placed at room temperature and stirred for 30 minutes in a nitrogen atmosphose, followed by reflux for 3 hours. After distillation, 50.3 g of 2,2,2-trifluoroethyl trifluoromethanesulfonate was obtained in yield of 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382687 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-5db3413241b240f089f8e33c9190bbf0 |
| Source note | uspto-grants-1995_01 |