Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375218Generated: November 1, 2026

Phenol → Cumene

https://huagongshe.com/reaction/1375218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantCumeneHCID 7406—
ReactantCumen hydroperoxideHCID 53627471—
SolventAcetoneHCID 180—
ProductCumeneHCID 7406—
ProductAcetophenoneHCID 7410—
Product2-Phenyl-2-propanolHCID 12053—

Reaction Steps

Phenol is manufactured via air oxidation of cumene to cumene hydroperoxide (CHP), followed by acid-catalyzed cleavage of CHP to phenol and acetone. CHP decomposition is a very exothermic reaction which is normally carried out on a commercial scale in continuous stirred or back-mixed reactors. In such reactors only a small fraction of CHP remains at any given time and the reaction medium consists essentially of the products of decomposition of CHP, i.e., phenol and acetone, plus any solvent (e.g., cumene) and other materials added with CHP to the reactor. During cumene oxidation small amounts of dimethyl phenyl carbinol (DMPC) and acetophenone are also formed. In the presence of acid catalyst, DMPC dehydrates to AMS, a useful by-product. Very high yields of AMS can be obtained from pure DMPC, e.g., 98 percent yield upon dehydration over acidic silica at 300° C. In the presence of phenol, however, and more specifically in phenol/acetone/cumene which is solvent in decomposition of technical CHP/DMPC mixtures, the AMS yield is normally about 50–60 mol percent of the DMPC. Main by-products are AMS dimers and cumylphenol which have no commercial value. Formation of cumylphenol also reduces the phenol yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166752B2
Source datasetuspto-grants-2007_01
ORD IDord-5f5ff82ae678493fb338f735c3eaf698
Source noteuspto-grants-2007_01