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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2219461Generated: October 30, 2026

Sodium Chloride → 1-(Benzyloxy)-2-bromo-4-fluorobenzene

https://huagongshe.com/reaction/2219461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-4-fluorophenolHCID 605472—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-(Benzyloxy)-2-bromo-4-fluorobenzeneHCID 2164090391%

Reaction Steps

To a mixture of 2-bromo-4-fluorophenol (24.7 g, 129 mmol), tetrabutylammonium iodide (4.8 g, 13.0 mmol), potassium carbonate (35.9 g, 260 mmol) and N,N-dimethylformamide (390 mL), benzyl bromide (23.5 g, 137 mmol) was added at room temperature and stirred for 1.5 hours. The reaction mixture was poured into a mixture of ethyl acetate and saturated aqueous sodium chloride, and then extracted with ethyl acetate. The organic phase was washed twice with saturated aqueous sodium chloride and then dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=90:10-80:20) to give 1-benzyloxy-2-bromo-4-fluoro-benzene (33.0 g, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07414072B2
Source datasetuspto-grants-2008_08
ORD IDord-a57c18d0a7374137a05320d751558bc8
Source noteuspto-grants-2008_08