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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727474Generated: October 26, 2026

Sulfuric Acid → 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-

https://huagongshe.com/reaction/727474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2,3,6-TrimethylphenolHCID 17016—
ReactantPotassium peroxymonosulphateHCID 10313463—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-HCID 7029174%

Reaction Steps

A solution of 13.6 g (100 mmol) of 2,3,6-trimethylphenol in 40 ml of acetic acid and a solution of 73.7 g (240 mmol) of 50% by weight potassium peroxomonosulfate in 320 ml of water were simultaneously added dropwise to a stirred solution of 0.68 g (2.0 mmol) of iron 5,14-dihydrodibenzo[b,i][5,9,14,18]tetraaza[14]annulene and 0.5 ml of concentrated sulfuric acid in 50 ml of acetic acid at room temperature with cooling. The reaction mixture was then subjected to steam distillation. The distillate was extracted by shaking with methylene chloride. The organic phase was shaken with aqueous sodium bicarbonate solution and then with water, separated from the aqueous phase, dried over magnesium sulfate, filtered and concentrated to a yellow oil, which slowly solidifed. 11.1 g (74%) of 2,3,5-trimethyl-p-benzoquinone were obtained in the form of yellow oily crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712416
Source datasetuspto-grants-1998_01
ORD IDord-9da68dad0b324541961fdd825f05dd61
Source noteuspto-grants-1998_01