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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854717Generated: November 1, 2026

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

https://huagongshe.com/reaction/1854717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-hydroxybenzaldehydeHCID 387179—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-bromobenzaldehydeHCID 1087002497%

Reaction Steps

To a suspension of 2-bromo-5-hydroxybenzaldehyde (100 mg, 0.50 mmol), potassium carbonate (138 mg, 1.00 mmol), and tetrabutylammonium iodide (18 mg, 0.05 mmol) in 1.0 mL of dry N,N-dimethylformamide was added benzyl bromide (89 μL, 0.74 mmol) at 0° C. After being stirred at room temperature overnight, the reaction mixture was diluted with diethyl ether, and the solution was washed with water, saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=95/5 to 80/20) to obtain the title compound as a colorless oil (140 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962674B2
Source datasetuspto-grants-2015_02
ORD IDord-ef04fd34d77646e492fb23eaa75f6b27
Source noteuspto-grants-2015_02