HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Hexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Pentene | HCID 8004 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Rhodium chloride | HCID 24872 | — |
| Reactant | Chlorotris(triphenylphosphine)rhodium(I) | HCID 84599 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-Hexanol | HCID 8103 | — |
| Product | 4-Methyl-1-pentanol | HCID 12296 | — |
| Product | Chlorotris(triphenylphosphine)rhodium(I) | HCID 84599 | — |
Reaction Steps
Chlorotris(triphenylphosphine)rhodium(I), [(03P)3RhCl], was prepared by refluxing an ethanol solution of rhodium(III) chloride in the presence of an excess amount of triphenylphosphine. Chlorotris(triphenylphosphine)rhodium(I) was dissolved in benzene, and the microspheres of Example III were added to the resulting red solution in an autoclave, equipped with a magnetic driven stirrer. Pentene-1 was introduced to the reactor along with benzene. The reaction was performed under conditions similar to Example IV. About 82% of the feed was reacted to give predominantly isohexanol and n-hexanol. The solid catalyst left inside of the reactor from this run was rinsed with fresh portions of benzene, and saved for another run.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03937742 |
| Source dataset | uspto-grants-1976_02 |
| ORD ID | ord-a139d5fb50024904a4df2e9a278658fa |
| Source note | uspto-grants-1976_02 |