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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836972Generated: November 1, 2026

4-Hydroxybenzoic Acid → 4-(Benzyloxy)benzoic acid

https://huagongshe.com/reaction/1836972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
CatalystTricaprylylmethyl ammonium chlorideHCID 77620884—
SolventMethanolHCID 887—
Product4-(Benzyloxy)benzoic acidHCID 7388055%

Reaction Steps

A solution of 4-hydroxybenzoic acid (5.52 g; 40 mole), benzyl bromide (11.89 mL; 0.1 mol) and tricaprylylmethylammonium chloride (100 mg, Aliquat 336® Henkel Corporation) in methanol (50 mL) was refluxed in presence of potassium carbonate (16.52 g) for 12 hours. The reaction mixture was then poured slowly into a solution of 2N hydrochloric acid solution. The precipitated acid was filtered, dried and recrystallized from hexane/ethyl acetate to give 5 g of 4-benzyloxybenzoic acid (yield=55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780865B1
Source datasetuspto-grants-2004_08
ORD IDord-16fe2370be994f8b8225dac321b5b242
Source noteuspto-grants-2004_08