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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604365Generated: October 30, 2026

Benzyl Bromide → 2-(Benzyloxy)-5-bromobenzaldehyde

https://huagongshe.com/reaction/1604365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromosalicylaldehydeHCID 72863—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(Benzyloxy)-5-bromobenzaldehydeHCID 73308790.9%

Reaction Steps

A solution of 5-bromosalicylaldehyde (12.0 g, 59.7 mmol) in DMF (50 ml) was treated with K2CO3 (16.5 g, 120 mmol) and benzyl bromide (11.2 g, 65.6 mmol). The reaction was stirred at ambient temperature for 18 hours. diluted with ethyl acetate and filtered. The filtrate was washed with HCl (0.05 M), saturated aqueous sodium hydrogen carbonate and brine. The organic phase was dried (Na2SO4) and evaporated and the residue triturated with hexane/ethyl ether. The product was filtered off to give 2-benzyloxy-5-bromobenzaldehyde as a white solid (15.8 g, 90%) m.p. 70-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994353
Source datasetuspto-grants-1999_11
ORD IDord-76e9e30e4f0645e0826ab6acd17b3220
Source noteuspto-grants-1999_11