HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844308Generated: October 31, 2026
Trifluoromethanesulfonic anhydride → 2,2-Difluoroethyl trifluoromethanesulfonate
https://huagongshe.com/reaction/1844308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2,2-Difluoroethan-1-ol | HCID 136187 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,2-Difluoroethyl trifluoromethanesulfonate | HCID 2774089 | 64.1% |
Reaction Steps
Triflic anhydride (27.9 g, 99.1 mmol) was placed in a flask and cooled with an ice bath. 2,2-Difluoroethanol (8.1 g, 99.1 mmol) was added and the reaction was heated to 84° C. for 1 hour. The reaction, was cooled in an ice bath and poured into 100 ml cold 5% NaHCO3 solution. The mixture was attracted with diethyl ether, dried over MgSO4, and concentrated under reduced pressure to remove the ether. The residue was vacuum distilled to give 2,2-difluoroethyl trifluoromethanesulfonate as a clear liquid (13.6 g, 64%, bp −55° C.). 1H NMR (400 MHz, CDCl3) δ ppm 6.17-5.88 (1H), 4.61-4.13 (2H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08946413B2 |
|---|
| Source dataset | uspto-grants-2015_02 |
|---|
| ORD ID | ord-1b106d1b53ef4ab082cb38b7c0cce862 |
|---|
| Source note | uspto-grants-2015_02 |
|---|