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 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1,1,4,4,4-Hexafluorobutane | HCID 67890 | 47% |
Reaction Steps
1,1,1,4,4,4-Hexafluoro-2-chloro-2-butene in 300 ml ethanol was hydrogenated in the presence of potassium hydroxide (12 g) and Raney nickel (25 g) at a temperature of 20° to 100° C. and under a pressure of 20 to 40 bar. The solid constituents were filtered off and the filtrate was extracted with water. The organic phase was separated and purified by distillation, giving 15.5 g (47% of theory) of 1,1,1,4,4,4-hexafluorobutane, boiling point 24°-27° C. at 1013 bar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931482 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-dc030f493b004efa8ee0518ef191d7de |
| Source note | uspto-grants-1990_06 |