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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658977Generated: November 2, 2026

Oxygen → 2,4,6-Trimethylphenol

https://huagongshe.com/reaction/1658977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
Reactant2,4,6-TrimethylphenolHCID 10698—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
Product2,4,6-TrimethylphenolHCID 10698—
Product4-Hydroxy-2,4,6-trimethylcyclohexa-2,5-dien-1-oneHCID 327234—

Reaction Steps

45 Parts of 2,4,6-trimethylphenol, 10 parts of sodium hydroxide, and 150 parts of water were fed to a stainless steel autoclave equipped with a gas-introducing pipe, temperature recorder and stirrer, and 100 Kg/cm2G oxygen pressure was applied. The reaction was conducted at 30°C. for 120 minutes, during which the pressure was reduced to 83 Kg/cm2G. The reaction product was recovered and extracted 2 times with 150 g of benzene with shaking. Analyses of benzene parts and water parts yielded 31.130 parts of 4-hydroxy-2,4,6-trimethyl-2,5-cyclohexadiene-1-one and 3.866 parts of unreacted 2,4,6-trimethylphenol from the benzene parts. 0.705 Parts of 4-hydroxy-2,4,6-trimethyl-2,5-cyclohexadiene-1-one and 0.090 parts of unreacted 2,4,6-trimethylphenol were also yielded from the water parts. Analyses of the results proved 91.2 % of conversion and 69.4 % of selectivity. Expelling the benzene out of said benzene solution and concentrating the benzene, 34 parts of oily product was obtained. The oily product was analyzed to be composed of 92.2 % of 4-hydroxy-2,4,6-trimethyl-2,5-cyclohexadiene-1-one and 9.6 % of 2,4,6-trimethylphenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03966818
Source datasetuspto-grants-1976_06
ORD IDord-e7c971c42705431c8dea4bf34ebdd609
Source noteuspto-grants-1976_06