HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,3,3-Tetrafluoro-1-propanol → 2,2,3,3-Tetrafluoropropyl 4-toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,3,3-Tetrafluoro-1-propanol | HCID 6441 | — |
| Reactant | 1,1-Dichloro-1,2,2,3,3-pentafluoropropane | HCID 61627 | — |
| Reactant | p-Toluenesulfonate chloride | HCID 22024621 | — |
| Product | 2,2,3,3-Tetrafluoropropyl 4-toluenesulfonate | HCID 2060597 | — |
Reaction Steps
Until HCFC-225cc becomes available in commercial quantities, HCFC-225cc may be prepared by a standard and well-known organic synthesis technique. For example, 1,1-dichloro-1,2,2,3,3-pentafluoropropane may be prepared by reacting 2,2,3,3-tetrafluoro-1-propanol and p-toluenesulfonate chloride to form 2,2,3,3-tetrafluoropropyl-p-toluenesulfonate. Next, the 2,2,3,3-tetrafluoropropyl-p-toluenesulfonate is reacted with potassium fluoride in N-methylpyrrolidone to form 1,1,2,2,3-pentafluoropropane. Then, the 1,1,2,2,3-pentafluoropropane is reacted with chlorine to form 1,1-dichloro-1,2,2,3,3-pentafluoropropane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116526 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-2c21630c313d42fc8e35fdab18cff644 |
| Source note | uspto-grants-1992_05 |