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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816335Generated: October 26, 2026

4-Cyclohexylcyclohexanol → (1,1'-Bicyclohexyl)-4-one

https://huagongshe.com/reaction/1816335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-CyclohexylcyclohexanolHCID 75518—
SolventAcetoneHCID 180—
Product(1,1'-Bicyclohexyl)-4-oneHCID 4169079.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-hydroxycyclohexylcyclohexane (25 g) in acetone (250 ml) was added dropwise with stirring 2.67N Jone's regend (77 ml) at 0° C. The mixture was then stirred for 1 hour at 0° C. The organic layer was collected and evaporated. The reaction mixture was added to a mixture of water and diethyl ether. The organic layer was washed with water, sodium hydrogen carbonate solution and brine. The organic layer was taken and dried over magnesium sulfate. The magnesium sulfate was filtered off, and the filtrate was concentrated under reduced pressure to give 4-cyclohexylcyclohexanone (19.57 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884774B2
Source datasetuspto-grants-2005_04
ORD IDord-6538edd7f04946fca2640004d114912b
Source noteuspto-grants-2005_04