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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234139Generated: October 26, 2026

Protocatechuic Acid → Benzyl 3,4-dihydroxybenzoate

https://huagongshe.com/reaction/234139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantProtocatechuic AcidHCID 72—
ReactantBenzyl AlcoholHCID 244—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium BicarbonateHCID 516892—
SolventBenzeneHCID 241—
ProductBenzyl 3,4-dihydroxybenzoateHCID 1665654153%

Reaction Steps

To the solution of 3,4-dihydroxybenzoic acid (1.13 g) in benzene (50 ml) were added benzyl alcohol (3.8 ml) and p-toluenesulfonic acid (139 mg), and the mixture was heated at reflux in the presence of Molecular Sieves 4A for 2 days. Further amount of benzyl alcohol (1.5 ml) was added. The mixture was then heated at reflux overnight. After cooling by standing, saturated aqueous sodium hydrogen carbonate was added. The mixture was extracted with ethyl acetate, washed with brine and dried over anhydrous magnesium sulfate. After the solvent was removed by distillation, the residue was dissolved in ethyl acetate and extracted with 1N sodium hydroxide. The aqueous layer was acidified with hydrochloric acid and extracted with ethyl acetate. After the organic layer was washed with brine, dried over anhydrous magnesium sulfate, the solvent was removed by distillation. The residue was purified by column chromatography on silica gel with an eluent system of chloroform:methanol=30:1 to give 953 mg of benzyl 3,4-dihydroxybenzoate (yield, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594004
Source datasetuspto-grants-1997_01
ORD IDord-abf98f2b22b647588b52d1c6f397b5d9
Source noteuspto-grants-1997_01