HuagongsheHuagongshe Chemistry Print Report · For research reference only
Vinylidene fluoride → 2-Trifluoromethyl-1,1,1,2,4,4-hexafluorobutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Vinylidene fluoride | HCID 6369 | — |
| Reactant | Butane, 1,1,1,4,4-pentafluoro-2-(trifluoromethyl)- | HCID 19888728 | — |
| Product | 2-Trifluoromethyl-1,1,1,2,4,4-hexafluorobutane | HCID 19931525 | — |
Reaction Steps
As another example, 2-trifluoromethyl-1,1,1,4,4-pentafluorobutane may be prepared by reacting commercially available 1,1-difluoroethylene according to the procedure of George L. Fleming et al., supra, to form a product which may then be hydrogenated to form 2-trifluoromethyl-1,1,1,2,4,4-hexafluorobutane which may then be dehydrohalogenated and then hydrogenated to form 2-trifluoromethyl-1,1,1,4,4-pentafluorobutane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05130345 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-00d582b5a898438da9c68dcac2bacc2c |
| Source note | uspto-grants-1992_07 |