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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247772Generated: October 30, 2026

Ethyl bromoacetate → Ethyl 2-(5-fluoro-2-nitrophenoxy)acetate

https://huagongshe.com/reaction/247772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant5-Fluoro-2-nitrophenolHCID 9937—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-(5-fluoro-2-nitrophenoxy)acetateHCID 1375280389.6%

Reaction Steps

To a mixture consisting of 5-fluoro-2-nitrophenol (47.1 g), acetonitrile (300 ml) and potassium carbonate (46 g) was added ethyl bromoacetate (60.1 g) dropwise at a temperature from 50° to 60° C., followed by a five-hour refluxing under heating and then filtration under cooling. The resulting filtrate was subjected to distillation under reduced pressure, and then dissolved in toluene (350 ml). The resulting toluene solution was washed with water, a 5% aqueous solution of potassium hydroxide, and water, in that order, followed by drying with magnesium sulfate and the toluene was distilled off therefrom under reduced pressure. The residue was distilled under reduced pressure to collect a fraction boiling at from 154° to 156° C., so as to obtain ethyl 5-fluoro-2-nitrophenoxyacetate (65.3 g). The whole quantity of the reaction product was dissolved in ethanol (8.1 l), followed by addition thereto of a solution of ammonium chloride (60 g) and water (400 ml). To the resulting mixture was added zinc dust (60.5 g) portionwise at a temperature of from 20° to 30° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05207818
Source datasetuspto-grants-1993_05
ORD IDord-dc388e3085664314a2d3ace37e34c634
Source noteuspto-grants-1993_05