HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene → 1,1,1,4,4,4-Hexafluorobutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-1,1,1,4,4,4-hexafluoro-2-butene | HCID 9815 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1,1,4,4,4-Hexafluorobutane | HCID 67890 | 47.8% |
Reaction Steps
In a stainless steel autoclave, 40 g of 1,1,1,4,4,4-hexafluoro-2-chloro-2-butene in 300 ml of ethanol were hydrogenated with hydrogen in the presence of 12 g of potassium hydroxide and 25 g of Raney nickel for 3 hours at 20° C. and another 1 hour at 100° C. at a pressure of from 30 to 40 bar. The solid components were then removed from the reaction mixture by filtration and the remaining liquid was distilled to give 16 g of 1,1,1,4,4,4-hexafluorobutane having a boiling point of 25°-30° C. at 1013 mbar. The mass spectrum showed a molecular ion at m/e 166.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04902839 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-2050e1b3e6fa446d89c89f99ed642da0 |
| Source note | uspto-grants-1990_02 |