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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605144Generated: November 2, 2026

2-Isopropylphenol → Cyclohexanol

https://huagongshe.com/reaction/1605144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IsopropylphenolHCID 6943—
ReactantPerhydroxyl radicalHCID 18500—
ReactantCumen hydroperoxideHCID 53627471—
SolventCyclohexaneHCID 8078—
ProductCyclohexanolHCID 7966—
ProductCyclohexanoneHCID 7967—
ProductCyclohexyl hydroperoxideHCID 69835—

Reaction Steps

A run was carried out in exactly the same manner as Run 10, except that the tertiary alcohol was cumenol and the tertiary hydroperoxide was cumene hydroperoxide. The mole ratio of cumenol to cyclohexane was 0.329:1 and the mole ratio of cumene hydroperoxide to cyclohexane was 0.086:1. A cyclohexyl hydroperoxide yield of 56 mole per cent, a cyclohexanol yield of 20 mole per cent, a cyclohexanone yield of 11 mole per cent and a residue of 13 mole per cent was obtained at a conversion level of 8.1 mole per cent and a per cent conversion rate of 5.8 per cent per hour. This run demonstrates that other tertiary alcohols and hydroperoxides are effective in the process of this invention.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03949003
Source datasetuspto-grants-1976_04
ORD IDord-4947925abe8c48258f5e3fe07f8b5fd3
Source noteuspto-grants-1976_04