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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081868Generated: November 2, 2026

Hydrochloric Acid → 2-(hydroxymethyl)-4-methoxyphenol

https://huagongshe.com/reaction/1081868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Hydroxy-5-methoxybenzaldehydeHCID 95695—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product2-(hydroxymethyl)-4-methoxyphenolHCID 48025377%

Reaction Steps

Under ice cooling, the solution of 5-methoxysalicylaldehyde (5 g) in ether (20 ml) was slowly added dropwise to the suspension of LiAlH4 (0.75 g) in ether (50 ml). After stirring at room temperature for 2 hours, another addition of LiAlH4 (0.5 g) was carried out under ice cooling, with subsequent stirring at room temperature for 30 minutes. To the reaction solution was added ice carefully, followed by sequential addition of 1N HCl and ether. After filtering off insoluble materials using Celite™, the ether layer was separated from the filtrate, and then, the aqueous phase was further extracted with ether. The combined ether layers were washed with saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was washed with ether-hexane and filtered to give the title compound (3.9 g; 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587392
Source datasetuspto-grants-1996_12
ORD IDord-3fd9f54b074d4167a284ff76df634988
Source noteuspto-grants-1996_12