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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472293Generated: October 30, 2026

Sulfuric Acid → 3,5-dihydroxy-4-methoxybenzyl alcohol

https://huagongshe.com/reaction/1472293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl GallateHCID 7428—
ReactantTetrahydrofuranHCID 8028—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3,5-dihydroxy-4-methoxybenzyl alcoholHCID 1609784236.6%

Reaction Conditions

Temperature62.5 °C

Reaction Steps

Next, a tetrahydrofuran solution (4 mL) with 4-methoxy form (560 mg, 2.8 mmol) with methyl gallate was dropped carefully to a tetrahydrofuran (THF) solution (6 mL) with lithium aluminum hydride (469 mg, 12.4 mmol) in an ice bath (0° C.). Then, the mixture was stirred for six hours at 60 to 65° C., ethyl acetate and a 10% sulfuric acid aqueous solution were added to the mixture, and then the reaction was stopped. Purified water was added to the reaction liquid, extraction was performed with the ethyl acetate, and the separated ethyl acetate layer was washed with saturated saline and dehydrated by sodium sulfate. After concentration, the extract liquid was purified by silica gel column chromatography (solvent: chloroform-methanol (50:1, v/v)→chloroform-methanol (50:3 , v/v)) and a reductant, that is, synthetic 3,5-dihydroxy-4-methoxybenzyl alcohol of 175.9 mg (yield: 36.6%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012513B2
Source datasetuspto-grants-2015_04
ORD IDord-455dd9a35639409cbea701cb97d7b4ff
Source noteuspto-grants-2015_04