HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975801Generated: October 26, 2026
2,2,3,3-Tetrafluoro-1-propanol → 2,2,3,3-Tetrafluoropropyl 4-toluenesulfonate
https://huagongshe.com/reaction/1975801
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1,3-Dichloro-1,1,2,2,3-pentafluoropropane | HCID 62353 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2,3,3-Tetrafluoropropyl 4-toluenesulfonate | HCID 2060597 | — |
Reaction Steps
Until HCFC-225cb becomes available in commercial quantities, HCFC-225cb may be prepared by a standard and well-known organic synthesis technique. For example, to prepare 1,3-dichloro-1,1,2,2,3-pentafluoropropane, 2,2,3,3-tetrafluoropropanol, tosyl chloride, and water are reacted together to form 2,2,3,3-tetrafluoropropyl p-toluenesulfonate. Then, N-methylpyrrolidone, potassium fluoride, and the 2,2,3,3-tetrafluoropropyl p-toluenesulfonate are reacted together to form 1,1,2,2,3-pentafluoropropane. Then, chlorine and the 1,1,2,2,3-pentafluoropropane are reacted to form 1,1,3-trichloro-1,2,2,3,2-pentafluoropropane. Finally, isopropanol and the 1,1,3-trichloro-1,2,2,3,2-pentafluoropropane are reacted to form 1,3-dichloro-1,1,2,2,3-pentafluoropropane. A detailed synthesis is set forth below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05288819 |
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| Source dataset | uspto-grants-1994_02 |
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| ORD ID | ord-572869c069e24eadb6c5f6bde326bb3a |
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| Source note | uspto-grants-1994_02 |
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