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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412155Generated: November 1, 2026

Acetone → Benzyl-2,4-bis-benzyloxy-5-bromobenzoate

https://huagongshe.com/reaction/2412155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2,4-dihydroxybenzoic acidHCID 81814—
SolventWaterHCID 962—
ProductBenzyl-2,4-bis-benzyloxy-5-bromobenzoateHCID 46915635—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a 10 L jacketed vessel, fitted with a flange lid containing stirrer, thermometer and dropping funnel, was charged acetone (2.5 L) followed by 5-bromo-2,4-dihydroxybenzoic acid (100 g, 0.43 mol) and potassium carbonate (356 g, 2.58 mol). To the stirring mixture at ambient was added benzyl bromide (185 mL, 1.55 mol) at a rate of 20 ml/min. The mixture was heated at 60° C. for 18 h and then taken to 45° C. Water (1.5 L) was added and the mixture stirred for 30 min. The mixture was extracted with EtOAc (2×1 L) and the combined organic portions reduced in vacuo. To the residue was added Et2O (200 mL) and petroleum ether (1 L), the mixture stirred for 30 min and the solid formed collected by filtration and dried in vacuo to give the title compound (197.2 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816087B2
Source datasetuspto-grants-2014_08
ORD IDord-f9a886512da040cba1e6ecd309818591
Source noteuspto-grants-2014_08