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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488907Generated: October 31, 2026

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

https://huagongshe.com/reaction/1488907

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 numberUS05677112
Source datasetuspto-grants-1997_10
ORD IDord-089a7c7353854b54be4708eee13adab0
Source noteuspto-grants-1997_10