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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057503Generated: October 31, 2026

4-Propylphenol → 4-Propylcyclohexanol

https://huagongshe.com/reaction/2057503

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PropylphenolHCID 12580—
Reactant4-PropylcyclohexanoneHCID 142482—
ReactantSodium ethoxideHCID 2723922—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product4-PropylcyclohexanolHCID 2775094—

Reaction Steps

In addition, the 4-propylcyclohexanone employed as a raw material in this preparation example was prepared as follows: A commercial p-n-propylphenol was hydrogenated in the presence of ethanol, sodium ethoxide and Raney nickel catalyst, under a hydrogen pressure of 100 atm, at 150° C. to form 4-n-propylcyclohexanol, which was then oxidized with Jones reagent (CrO3 /H2SO4 /H2O) in acetone to obtain 4-n-propylcyclohexanone having a b.p. of 110°~113° C./26 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04211666
Source datasetuspto-grants-1980_07
ORD IDord-45510c2c41bc4e43beb9d27e9af245af
Source noteuspto-grants-1980_07