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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181082Generated: November 2, 2026

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

https://huagongshe.com/reaction/1181082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant2-Bromo-5-hydroxybenzaldehydeHCID 387179—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-bromobenzaldehydeHCID 10870024—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-bromo-5-hydroxy-benzaldehyde (5.99 g, 29.8 mmol, Preparation 13 Step A) in DMF (50 mL) was treated with benzyl bromide (7.65 g, 44.7 mmol) and Cs2CO3 (15.1 g, 44.7 mmol). The resulting mixture was heated at 80° C. for 60 min and was quenched with water (200 mL). The mixture was extracted with EtOAc (2×100 mL), dried (Na2SO4), and concentrated to a residue, which was purified on silica gel chromatography (hexanes/EtOAc 9/1) to afford 5-benzyloxy-2-bromo-benzaldehyde as white solid in quantitative yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282501B2
Source datasetuspto-grants-2007_10
ORD IDord-dbb74fd82e4a456ca3ea87b9e56004b9
Source noteuspto-grants-2007_10