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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901136Generated: October 29, 2026

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

https://huagongshe.com/reaction/1901136

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzoic AcidHCID 135—
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
SolventAcetoneHCID 180—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-(Benzyloxy)benzoic acidHCID 7388071.2%

Reaction Steps

A suspension of p-hydroxybenzoic acid (200 g, 1.2 mole), benzyl chloride (190 g, 1.5 mole) and potassium carbonate (165 g, 1.2 mole) in acetone (1200 ml) was reacted with stirring for 12 hours under reflux. After cooling, the precipitate was filtered off, and the filtrate was concentrated until 400 ml. H2O (1 l) was added with stirring to the residue and the mixture was allowed to stand. The organic layer separated was concentrated. The residue was added to a solution of NaOH (60 g, 1.5 mole) in H2O (1 l) and ethanol (500 ml), and stirred for 4 hours and dissolved. Then conc. hydrochloric acid (200 ml) was added to make pH 1. The precipitate was filtered, washed with H2O and with ethanol, and dried to give 195 g of 4-benzyloxybenzoic acid as white crystals having a m.p. of 191.2°-192.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576359
Source datasetuspto-grants-1996_11
ORD IDord-d93105c9ce2c4f42a2ed69f54029c1c4
Source noteuspto-grants-1996_11