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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477424Generated: October 26, 2026

2,4-Di-tert-butylphenol → Cyclohexanone, 2,4-bis(1,1-dimethylethyl)-

https://huagongshe.com/reaction/477424

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Di-tert-butylphenolHCID 7311—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
ProductCyclohexanone, 2,4-bis(1,1-dimethylethyl)-HCID 11444271.3%

Reaction Steps

300 g of 2,4-di-tert-butylphenol and 3.0 g of 5% palladium-carbon catalyst were introduced into a 500 ml autoclave and stirred therein at a reaction temperature of 180° C. under a hydrogen pressure of 20 kg/cm2. After approximately ten hours, the absorption of the theoretical amount (2.9 moles) of hydrogen was confirmed. Then the reaction mixture was cooled to room temperature and the catalyst was filtered off. 218 g of the crude 2,4-di-tert-butylcyclohexanone thus obtained was distilled under reduced pressure in a Helipack packing column of a number of theoretical plates of 5 to give 245 g of a colorless and transparent 2,4-di-tert-butylcyclohexanone (I) fraction (b.p.: 93° to 94° C./3 mm Hg). It was confirmed by gas chromatography that this product was a mixture of cisisomer (I-A) and trans-isomer (I-B) at a ratio of 83:17. The physical properties of this product were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04888323
Source datasetuspto-grants-1989_12
ORD IDord-0792d2a5cd53401794f6cacc7953f916
Source noteuspto-grants-1989_12