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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412147Generated: October 31, 2026

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

https://huagongshe.com/reaction/2412147

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 numberUS08816087B2
Source datasetuspto-grants-2014_08
ORD IDord-d4d55f7a4dd5450b8096076d78e1eeda
Source noteuspto-grants-2014_08