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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297559Generated: October 30, 2026

Phenol → Cyclohexanol

https://huagongshe.com/reaction/1297559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantCyclohexanoneHCID 7967—
ReactantPhenol cyclohexaneHCID 21202897—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178515949HCID 178515949—
CatalystPalladiumHCID 23938—
SolventCyclohexaneHCID 8078—
ProductPhenolHCID 996—
ProductCyclohexanolHCID 79662%

Reaction Steps

In the case of hydrogenating phenol through a phenol hydrogenation process of prior art, for example by using an alumina-supported palladium catalyst, and introducing a mixed solution of phenol and cyclohexane with a phenol/cyclohexane molar ratio of ½ at a phenol flow rate of 0.0135 mol/hr into a hydrogen gas stream (hydrogen/phenol molar ratio=5.4) and carrying out reaction at 230° C., at the start of the flow reaction 98% cyclohexanone and 2% cyclohexanol were produced at a phenol conversion ratio of 77%. However, with this method, there is a drawback that a drop in activity and hence a drop in the conversion ratio occurs due to carbonaceous matter accumulating on the catalyst, and hence the conversion ratio became 63% thirty minutes after the start of the reaction, 55% after 1 hour, 44% after 2 hours, and 42% after 8 hours. Moreover, with this method, experimental operation using only phenol was difficult, and hence the phenol had to be used with harmful cyclohexane as a solvent (N. Mahata and V. Vishwanathan, Journal of Catalysis, 196, 262-270 (2000)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250537B2
Source datasetuspto-grants-2007_07
ORD IDord-db1299e6a46949fba6e445f8473a9ad0
Source noteuspto-grants-2007_07