HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668268Generated: October 31, 2026
2,2,3,3-Tetrafluoro-1-propanol → 2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonate
https://huagongshe.com/reaction/1668268
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl fluoride, trifluoro- | HCID 67631 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,2,3,3-Tetrafluoropropyl trifluoromethanesulfonate | HCID 3792475 | — |
Reaction Steps
2,2,3,3-tetrafluoropropan-1-ol (244.3 g, 1.85 mol, obtained from Sinochem Corp.), triethylamine (187.2 g, 1.85 mol, obtained from Aldrich Chemical Co.) and 500 mL of chloroform were combined in a 2-liter Parr pressure reactor and sealed. The reactor temperature was set to −10° C. Trifluoromethanesulfonyl fluoride (281.33 g, 1.85 mol, obtained from 3M Company) was added at such a rate that the temperature did not exceed −5° C. Once the addition was complete, the mix was held at −10° C. for 45 minutes. The reaction mix was then emptied and washed with 2×500 mL portions of water and 1×250 mL portion of 1N HCl. GC analysis of the reaction mixture indicated a 97 percent conversion to the product. The chloroform solvent was removed by rotary evaporation. The product was dried over anhydrous magnesium sulfate which was then filtered from the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07988877B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-4f99390ce87f463fb161039acb11fac7 |
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| Source note | uspto-grants-2011_08 |
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