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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253950Generated: November 1, 2026

Isopropanol → Cyclooctane

https://huagongshe.com/reaction/2253950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactantcis,cis-1,5-CyclooctadieneHCID 8135—
CatalystTetrarhodium dodecacarbonylHCID 9940312—
SolventAcetoneHCID 180—
ProductCyclooctaneHCID 9266—
Product1-CycloocteneHCID 13609—

Reaction Steps

0.3 ml of 1,5-cyclooctadiene, 32 ml of 2propanol, 8 ml of acetone, 0.5 mg of ferric 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 apapratus as an outer light source and passed through a filter UV-25, mfd. by Toshiba Corporation, were used in the irradiation. After the irradiation was conducted for 5 hours in such a manner, the reaction solution was analyzed by gas chromatography. Cyclooctene was obtained in a yield of 95% with the formation of cyclooctane in a yield of 5%. No unreacted 1,5-cyclooctadiene was detected by the gas chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233110
Source datasetuspto-grants-1993_08
ORD IDord-ab0335a1520e4c509d20a3e0b9ebe5fd
Source noteuspto-grants-1993_08