HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1200205Generated: October 30, 2026
3-Methoxyphenol → 2-Methoxy-1,4-benzoquinone
https://huagongshe.com/reaction/1200205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methoxyphenol | HCID 9007 | — |
| Reactant | Potassium nitrosodisulfonate | HCID 3032624 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methoxy-1,4-benzoquinone | HCID 76146 | 117.5% |
Reaction Steps
A solution of potassium nitrosodisulfonate (0.75 g) and potassium monobasic phosphate (0.75 g) in water (37.5 ml) was added to m-methoxyphenol (109 mg, 0.9 mmol) in acetone (12.5 ml) and the resulting mixture was stirred vigorously for 10 minutes. Potassium nitrosodisulfonate (0.75 g) was added to the reaction mixture in two portions at 30 minute intervals and the stirring was continued for an additional two hours. After removal of acetone under reduced pressure, the resulting aqueous solution was extracted with dichloromethane (four 10 ml aliquots). The combined organic layers were washed with 0.01 N sodium hydroxide (10 ml) and then with water (10 ml) and then dried over anhydrous magnesium sulfate. The dried solution was filtered and the solvents removed under reduced pressure to yield 146.1 mg of 2 -methoxy-p-benzoquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04904764 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-ab2084d635c246d29f5da04905e088a5 |
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| Source note | uspto-grants-1990_02 |
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