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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854691Generated: November 3, 2026

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

https://huagongshe.com/reaction/1854691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2-nitrobenzaldehydeHCID 39211—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-nitrobenzaldehydeHCID 384983587.5%

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 for 5 h, the reaction mixture was filtrated 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 pale yellow solid (405 mg, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962674B2
Source datasetuspto-grants-2015_02
ORD IDord-c8f13f9d998e41ec876c9e74109e287b
Source noteuspto-grants-2015_02