HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19322Generated: October 26, 2026
Triethylamine → 2,2-Difluoroethyl trifluoromethanesulfonate
https://huagongshe.com/reaction/19322
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2,2-Difluoroethan-1-ol | HCID 136187 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Difluoroethyl trifluoromethanesulfonate | HCID 2774089 | 75% |
Reaction Steps
In a flask under argon was placed triflic anhydride (10.22 mL, 61 mmol) and dichloromethane (10 mL) and it was cooled to −70° C. To this cooled mixture was added slowly a solution of 2,2-difluoroethanol (5.00 g, 61 mmol) and triethylamine (8.5 mL, 61 mmol) in dichloromethane (10 mL). After the addition was complete, the mixture was warmed to 25° C. and then concentrated in vacuo. This material was distilled at 60° C. and 50 mm Hg which afforded trifluoro-methanesulfonic acid 2,2-difluoro-ethyl ester (9.74 g, 75%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741327B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-7ce4d0728fee45208e0af46ba190a52b |
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| Source note | uspto-grants-2010_06 |
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