HuagongsheHuagongshe Chemistry Print Report · For research reference only
Perfluoropropyl iodide → HCID 178448065, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Perfluoropropyl iodide | HCID 33977 | — |
| Reactant | HCID 178447857 | HCID 178447857 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 178448065 | HCID 178448065 | — |
Reaction Steps
A mixture of 0.1 mol of 4-(trans-4-propylcyclohexyl)-cyclohex-1-ene, 0.1 mol of heptafluoropropyl iodide, 10 mol % of tetrakis-(triphenylphosphine)-palladium and 200 ml of hexane is heated under reflux for 24 hours (compare T. Ishihara, Chemistry Letters (1986) 1895). The isomer mixture of the addition product thus formed is, after the catalyst has been filtered off, first heated with tributyl-tin hydride for 90 hours in toluene and reduced. The all-trans product>.trans-4-(trans-4-propylcyclohexyl)-1-heptafluoropropylcyclohexane, is finally obtained by separating the thiourea inclusion compound from a solution in methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05348677 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-eebc84b8072b4261b919be9dc41d8084 |
| Source note | uspto-grants-1994_09 |