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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395052Generated: October 29, 2026

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

https://huagongshe.com/reaction/2395052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-BromosalicylaldehydeHCID 72863—
SolventDimethylformamideHCID 6228—
Product2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—

Reaction Steps

A mixture of 5-bromosalicylaldehyde (12 g), potassium carbonate (16.5 g) and benzyl bromide (7.8 ml) in DMF (50 ml) was stirred for 18 hours, poured into ethyl acetate (100 ml), washed with 0.05M HCl (100 ml), sodium bicarbonate (100 ml) and brine (100 ml), dried (sodium sulphate), filtered and evaporated. The residue was triturated with hexane/diethyl ether to give 2-benzyloxy-5-bromo-benzaldehyde (15.8 g) mp.70°-72° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811459
Source datasetuspto-grants-1998_09
ORD IDord-94d50fc8377248998528525ffd7c757a
Source noteuspto-grants-1998_09