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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177190Generated: November 1, 2026

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

https://huagongshe.com/reaction/1177190

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, 17 H), 5.38 (s, 2 H), 5.21 (s, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-a8689795cbe640e8b860726e9b7b5351
Source noteuspto-grants-2010_11