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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625405Generated: November 1, 2026

Benzyl Bromide → Methyl 5-acetyl-2,4-bis-benzyloxybenzoate

https://huagongshe.com/reaction/1625405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-acetyl-2,4-dihydroxybenzoateHCID 12482079—
SolventAcetonitrileHCID 6342—
ProductMethyl 5-acetyl-2,4-bis-benzyloxybenzoateHCID 1195586999%

Reaction Steps

Benzyl bromide (70 ml, 0.59 mol) was added to a stirred mixture of methyl 5-acetyl-2,4-dihydroxybenzoate (60.7 g, 0.29 mol) and anhydrous potassium carbonate (87.8 g, 0.64 mol) in acetonitrile (800 ml) and the mixture was stirred and held at reflux for 16 hours. Upon cooling to room temperature the mixture was poured onto water (3 L) and stirred vigorously for 2 hours. The solids were collected by filtration, rinsed with water (2 L), sucked dry under reduced pressure and dried to constant mass in a vacuum oven at 60° C. overnight to afford methyl 5-acetyl-2,4-bis-benzyloxybenzoate (112.1 g, 99%) as a cream solid. 1H NMR (DMSO-d6) 8.21 (1H, s), 7.55 (4H, m), 7.43 (4H, m), 7.37 (2H, m), 7.04 (1H, s), 5.38 (4H, s), 3.79 (3H, s), 2.48 (3H, s). MS: [M+H]+ 391.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779132B2
Source datasetuspto-grants-2014_07
ORD IDord-32068c8f98b646b496c4115aec6d20d1
Source noteuspto-grants-2014_07