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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253952Generated: November 1, 2026

Isopropanol → Cyclooctane

https://huagongshe.com/reaction/2253952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
Reactantcis,cis-1,5-CyclooctadieneHCID 8135—
CatalystTetrarhodium dodecacarbonylHCID 9940312—
CatalystHCID 23169391HCID 23169391—
SolventAcetoneHCID 180—
ProductCyclooctaneHCID 9266—
Product1-CycloocteneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05233110
Source datasetuspto-grants-1993_08
ORD IDord-027c9d703c6c472f8c74d12c0df4523b
Source noteuspto-grants-1993_08