Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670Generated: October 26, 2026

Benzyl Bromide → Methyl 4-(benzyloxy)-2-hydroxybenzoate

https://huagongshe.com/reaction/1670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2,4-DihydroxybenzoateHCID 16523—
SolventAcetoneHCID 180—
ProductMethyl 4-(benzyloxy)-2-hydroxybenzoateHCID 225489—

Reaction Steps

To a stirred, 0° C. solution of methyl 2,4-dihydroxybenzoate (50 g, 300 mmol) in acetone (1000 mL) was added K2CO3 (150 g, 1000 mmol) and benzyl bromide (330 mmol, 39 mL). The solution was allowed to warm to ambient temperature over 48 h. The reaction solution was filtered through celite and the acetone solution stripped down under reduced pressure. The crude oil was dissolved in EtOAc (1000 mL) and washed with water (250 mL), and saturated aqueous NaHCO3 (500 mL). The EtOAc layer was dried (MgSO4), filtered, and the EtOAc was removed under reduced pressure. The crude product was purified by pressurized silica gel column chromatography using 5:1 hexanes:EtOAc. Evaporation of the hexanes:EtOAc mixture gave the desired methyl 4-benzyloxy-2-hydroxybenzoate as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726172
Source datasetuspto-grants-1998_03
ORD IDord-b4fd402e735143d2ba1df2c8a9a0fe8f
Source noteuspto-grants-1998_03