HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2-Difluoroethyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2,2-Difluoroethan-1-ol | HCID 136187 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,2-Difluoroethyl trifluoromethanesulfonate | HCID 2774089 | — |
Reaction Steps
With cooling with ice, 2.7 ml of trifluoromethanesulfonic acid anhydride was added to a chloroform (100 mL) solution of 1 mL of 2,2-difluoroethanol and 2.2 mL of triethylamine, and stirred for 30 minutes. The reaction liquid was diluted with chloroform, and washed with aqueous saturated sodium bicarbonate solution and saturated saline water in that order. The organic layer was dried with anhydrous magnesium sulfate, and the solvent was evaporated away under reduced pressure to obtain the entitled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436004B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-aff4da5c4bac4de38d332dec9525f31e |
| Source note | uspto-grants-2013_05 |