HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979666Generated: October 30, 2026
Hydrogen Peroxide → 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-
https://huagongshe.com/reaction/1979666
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 2,3,6-Trimethylphenol | HCID 17016 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl- | HCID 70291 | 84% |
Reaction Steps
600 mg of the catalyst prepared in Example 6 and 10 g of 2,3,6-trimethylphenol were added to 90 ml of acetic acid. While cooling the solution with ice water, 20 g of a 30% hydrogen peroxide aqueous solution was dropwise added in about 40 minutes, and the mixture was stirred overnight. After completion of the reaction, the catalyst was removed by filtration, and the acetic acid solution was concentrated under reduced pressure to about 20 ml, diluted with ether, washed with an aqueous solution of NaHCO3 and then dried. The ether was distilled off, and the residue was subjected to distillation under reduced pressure, whereby 8.7 g of trimethylbenzoquinone (boiling point: 64° C./0.7 torr) was obtained. Further, the distillation residue was treated by column chromatography (SiO2 /CH2Cl2), whereby 0.5 g of trimethylbenzoquinone was additionally obtained. The total amount was 9.2 g (84% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04482493 |
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| Source dataset | uspto-grants-1984_11 |
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| ORD ID | ord-001e681fde9b4de5a1299e4bc074c077 |
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| Source note | uspto-grants-1984_11 |
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