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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfuric AcidHCID 1118—
ReactantDiethyl EtherHCID 3283—
Reactant4,5-DimethylresorcinolHCID 10697—
ReactantSodium HydroxideHCID 14798—
ReactantPotassium PermanganateHCID 516875—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
ProductBenzaldehyde, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04975455
Source datasetuspto-grants-1990_12
ORD IDord-3ed6ddd7045b4f858a1bbc113bceab8b
Source noteuspto-grants-1990_12