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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040381Generated: October 26, 2026

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

https://huagongshe.com/reaction/1040381

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-nitrobenzaldehydeHCID 3849835—

Reaction Steps

To a suspension of 5-hydroxy-2-nitrobenzaldehyde (300 mg, 1.80 mmol), potassium carbonate (498 mg, 3.60 mmol), and tetrabutylammonium iodide (66 mg, 0.18 mmol) in 1.8 mL of dry N,N-dimethylformamide was added benzyl bromide (0.32 mL, 2.7 mmol) at 0° C. After being stirred at room temperature until the starting material disappeared (5 h), the reaction mixture was filtered to remove inorganic salts. The filtrate 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=90/10 to 75/25) to obtain the title compound as a slightly yellow solid (405 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552220B2
Source datasetuspto-grants-2013_10
ORD IDord-ecea00dc8af24c10a89f28789974b9a3
Source noteuspto-grants-2013_10