HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1,1,1,4,4,4-Hexafluorobutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 3804140 | HCID 3804140 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,1,1,4,4,4-Hexafluorobutane | HCID 67890 | 59% |
Reaction Steps
1,1,1,4,4,4-Hexafluoro-2-bromo-3-chloro-2-butene (10 g, 36 mmole) in 50 ml tetrahydrofuran was hydrogenated in the presence of sodium hydroxide (3.0 g) and Raney nickel (5 g) at a temperature of 20° to 40° C. and under a hydrogen pressure of 20 to 40 bar. The reaction mixture was worked up as in Example B, producing 3.5 g (59% of theory) of 1,1,1,4,4,4-hexafluorobutane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931482 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-383a294a029d4590927525520f29b8df |
| Source note | uspto-grants-1990_06 |