HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706694Generated: November 1, 2026
Hydrogen Peroxide → 1,2-Benzenediol, 4-methoxy-
https://huagongshe.com/reaction/1706694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2-Hydroxy-4-Methoxybenzaldehyde | HCID 69600 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,2-Benzenediol, 4-methoxy- | HCID 587766 | — |
Reaction Steps
4-methoxycatechol was prepared by the method described in Organic Synthesis, Collective Volume 3, page 759: 60.8 g of 4-methoxysalicylaldehyde was added to a stirred solution of 16 g of sodium hydroxide in 200 ml of water. Under nitrogen gas, a solution of 60 g of 30% hydrogen peroxide in water dissolved in 200 ml of water was added drop-by-drop to the resulting solution, held at 35°-40° C. Then sodium sulfate (and a small amount of sodium hydrosulfite to decolorize the mixture) was added until the mixture was saturated. The mixture was extracted with methylene chloride. The resulting residue was extracted with ether. The ether extract was dried (Na2SO4, Na2S2O4) and the solvent was evaporated under reduced pressure, to give crude 4-methoxycatechol (10A).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04208424 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-a8e1c1a18b27497f8a9d26da803780ae |
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| Source note | uspto-grants-1980_06 |
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