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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060095Generated: October 30, 2026

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

https://huagongshe.com/reaction/2060095

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 11955869142.8%

Reaction Steps

Methyl 5-acetyl-2,4-dihydroxybenzoate (2.62 g, 12.48 mmol) was dissolved in acetonitrile (40 ml), anhydrous potassium carbonate (4.93 g, 35.7 mmol) was added and the stirred mixture was treated with benzyl bromide (5.09 g, 29.75 mmol) and held at reflux for 3 hours. Upon cooling the solvent was removed in vacuo and the mixture partitioned between water and dichloromethane. The organic layer was separated and the solvent removed in vacuo to afford methyl 5-acetyl-2,4-bis-benzyloxybenzoate (3.48 g, 71%) as a colourless solid which was dried at 50° C. in a vacuum oven and used without further purification. 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 numberUS08277807B2
Source datasetuspto-grants-2012_10
ORD IDord-618e11886b56424b9f9b98855aef0570
Source noteuspto-grants-2012_10