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 | 2-Trifluoromethyl-1,1,1,4,4-pentafluoro-2-butanol | HCID 19788888 | — |
| Product | 2-Trifluoromethyl-1,1,1,2,4,4-hexafluorobutane | HCID 19931525 | — |
Reaction Steps
As another example, 2-trifluoromethyl-1,1,1,4,4-pentafluoro-2-butanol 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 reacted with sulfuric acid and then water to form 2-trifluoromethyl-1,1,1,4,4-pentafluoro-2-butanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05254755 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-0b1f8c74536e4d0db36efb794058873e |
| Source note | uspto-grants-1993_10 |