Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | cis,cis-1,5-Cyclooctadiene | HCID 8135 | — |
| Catalyst | Tetrarhodium dodecacarbonyl | HCID 9940312 | — |
| Catalyst | HCID 23169391 | HCID 23169391 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Cyclooctane | HCID 9266 | — |
| Product | 1-Cyclooctene | HCID 13609 | — |
Reaction Steps
0.3 ml of 1,5-cyclooctadiene, 32 ml of 2-propanol, 8 ml of acetone, 2.2 mg of nickel nitrate hydrate and 3 mg of tetrarhodiumdodecacarbonyl [Rh4 (CO)12 ] were fed into the same quartz cell as that used in the Example 1. Nitrogen gas was bubbled through the contents under stirring for 10 minutes and thereafter, the irradiation of the cell with light was started. The stirring was conducted with a magnetic stirrer. The reaction cell was put in a quartz-window thermostatic chamber to keep the reaction temperature at 20° C. The rays which were emitted from a 500-W high-pressure mercury lamp set on an irradiation apparatus as an outer light source and passed through a filter UV-25, mfd. by Toshiba Corporation, were used in the irradiation. After the irradiation had been conducted for 5 hours in such a manner, the reaction solution was analyzed by gas chromatography. Cyclooctene was obtained in a yield of 93% with the formation cyclooctane in a yield of 3%. 4% of unreacted 1,5-cyclooctadiene remained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05233110 |
|---|
| Source dataset | uspto-grants-1993_08 |
|---|
| ORD ID | ord-027c9d703c6c472f8c74d12c0df4523b |
|---|
| Source note | uspto-grants-1993_08 |
|---|