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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1940381Erstellt: 26. Oktober 2026

Protocatechuic Acid → Benzyl 3,4-dihydroxybenzoate

https://huagongshe.com/reaction/1940381

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktProtocatechuic AcidHCID 72—
EduktBenzyl AlcoholHCID 244—
Eduktp-Toluenesulfonic acidHCID 6101—
EduktSodium BicarbonateHCID 516892—
LösungsmittelBenzeneHCID 241—
ProduktBenzyl 3,4-dihydroxybenzoateHCID 1665654153%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05698692
Quelldatensatzuspto-grants-1997_12
ORD IDord-1df0b3e666074f419ab4f2332ebb1962
Quellennotizuspto-grants-1997_12