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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026556Generated: October 31, 2026

Benzyl Bromide → Benzyl 4-bromo-2-fluorobenzoate

https://huagongshe.com/reaction/1026556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-2-fluorobenzoic acidHCID 302681—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-bromo-2-fluorobenzoateHCID 22351348—

Reaction Conditions

Temperature60 °C

Reaction Steps

To an N,N-dimethylformamide solution (400 ml) of 4-bromo-2-fluorobenzoic acid (50.3 g) were added at room temperature potassium carbonate (63.5 g) and benzyl bromide (27.3 ml), followed by stirring at 60° C. for 3 hours. After the precipitate was filtered off, the filtrate was concentrated to 100 ml, and then diluted with ethyl acetate. This was washed sequentially with a saturated aqueous ammonium chloride solution, water and saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to afford benzyl 4-bromo-2-fluorobenzoate (70.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729095B2
Source datasetuspto-grants-2014_05
ORD IDord-e5017ad252c7482f80f369444ff108c9
Source noteuspto-grants-2014_05