Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424039Generated: October 28, 2026

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

https://huagongshe.com/reaction/424039

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 numberUS08101648B2
Source datasetuspto-grants-2012_01
ORD IDord-6ccfca115acd4280aefa4cf174081010
Source noteuspto-grants-2012_01