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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163536Generated: October 29, 2026

Ethyl bromoacetate → Ethyl 2-(4-nitrophenoxy)acetate

https://huagongshe.com/reaction/1163536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant3-NitrophenolHCID 11137—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductEthyl 2-(4-nitrophenoxy)acetateHCID 30893892%

Reaction Steps

A dry reaction flask equipped with a reflux condenser, N2 inlet and a magnetic stirring bar was charged with 3-nitrophenol (76.45 g, 550 mmol), K2CO3 (76.45 g, 550 mmol) and dry acetone (500 mL) under N2 atmosphere. To this at room temperature was added ethyl bromoacetate (55.44 mL, 500 mmol) over a period of 15 min. The reaction mixture was refluxed for 16 h, cooled and poured over ice-water (4 Kg). The resulting aqueous solution was extracted with CH2Cl2 (3×500 mL), dried over anhydrous Na2SO4 and solvent was removed to obtain 103 g (92%) of the desired ethyl 4-nitrophenoxyacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820819B2
Source datasetuspto-grants-2010_10
ORD IDord-ee33a92e8daf4f7faafbd62138e0e143
Source noteuspto-grants-2010_10