HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110416Generated: November 2, 2026
Hydrochloric Acid → Benzaldehyde, 4,6-dihydroxy-2,3-dimethyl-
https://huagongshe.com/reaction/1110416
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4,5-Dimethylresorcinol | HCID 10697 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Product | Benzaldehyde, 4,6-dihydroxy-2,3-dimethyl- | HCID 254155 | — |
Reaction Steps
4.450 g (32 mmol) of 2,3-dimethyl-5-hydroxyphenol are dissolved in 100 ml of anhydrous ethyl ether in a round-bottomed flask equipped with a gas inlet, a thermometer and a condenser (the outflow gases being trapped by 3 successive bubblers: H2SO4, saturated KMnO4 solution, 3N NaOH). After 5.635 g (48 mmol) of zinc cyanide have been added, a stream of gaseous hydrochloric acid is passed through for 2 hours with stirring at room temperature. A copious precipitate appears, increasing with the passage of time. At the end of the operation, a powerful stream of nitrogen is passed through the reaction medium. The insoluble matter is separated by filtration and dissolved in boiling water. After cooling, the aldehyde precipitates. After filtration, the crystals are washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04975455 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-3ed6ddd7045b4f858a1bbc113bceab8b |
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| Source note | uspto-grants-1990_12 |
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