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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643664Generated: November 2, 2026

Benzyl Bromide → Benzyl 3,5-bis(benzyloxy)-4-bromobenzoate

https://huagongshe.com/reaction/1643664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-3,5-dihydroxybenzoic acidHCID 86023—
SolventDimethylformamideHCID 6228—
ProductBenzyl 3,5-bis(benzyloxy)-4-bromobenzoateHCID 1005181359.6%

Reaction Steps

To a stirred solution of 4-bromo-3,5-dihydroxy-benzoic acid (350 g, 1.5 mol) in dry DMF (2 L) were added K2CO3 (725 g, 5.25 mL) and BnBr (769 g, 4.5 mol) in one portion. The mixture was stirred at room temperature for 2 days and then filtered. The filter cake was washed with CH2Cl2. The combined filtrates were concentrated to give the title compound (225 g, 40% yield) as a white solid. 1H NMR (400 MHz, CDCl3): δ 7.22-7.52 (m, 17H), 5.38(s, 2H), 5.21 (s, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-6835b46d76cb46e49b60e3ce76b6c4df
Source noteuspto-grants-2012_02