HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,3,3,3-Pentafluoropropanol → 2,2,3,3,3-Pentafluoropropyl p-Toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,3,3,3-Pentafluoropropanol | HCID 9872 | — |
| Reactant | 3,3-Dichloro-1,1,1,2,2-pentafluoropropane | HCID 61112 | — |
| Reactant | HCID 22024621 | HCID 22024621 | — |
| Product | 2,2,3,3,3-Pentafluoropropyl p-Toluenesulfonate | HCID 2776017 | — |
Reaction Steps
Until HCFC-225ca becomes available in commercial quantities, HCFC-225ca may be prepared by a standard and well-known organic synthesis technique. For example, to prepare 1,1-dichloro-2,2,3,3,3-pentafluoropropane, 2,2,3,3,3-pentafluoro-1-propanol and p-toluenesulfonate chloride are reacted together to form 2,2,3,3,3-pentafluoropropyl-p-toluenesulfonate. Then, N-methylpyrrolidone, lithium chloride, and the 2,2,3,3,3-pentafluoropropyl-p-toluenesulfonate are reacted together to form 1-chloro-2,2,3,3,3-pentafluoropropane. Chlorine and the 1-chloro-2,2,3,3,3-pentafluoropropane are then reacted together to form 1,1-dichloro-2,2,3,3,3-pentafluoropropane. A detailed synthesis is set forth below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05116526 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-4a1bbb71ea364898b9da00dbfb31be0b |
| Source note | uspto-grants-1992_05 |