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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435848Generated: November 1, 2026

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

https://huagongshe.com/reaction/1435848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxy-3-nitrobenzaldehydeHCID 18169—
SolventDimethylformamideHCID 6228—
Productethyl 2-(4-formyl-2-nitrophenoxy)acetateHCID 5305379—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 4-hydroxy-3-nitrobenzaldehyde (6.9 g) and ethyl bromoacetate (5.0 mL) in dimethylformamide (250 mL) was treated with anhydrous potassium carbonate (10 g) and the mixture was heated at 60° C. for 18 hours and evaporated to dryness. The residue was partitioned between water and diethyl ether, and the diethyl ether layer was washed with 0.5M sodium hydroxide. It was then dried over anhydrous sodium sulfate and evaporated to give an oil that was chromatographed on silica gel (ethyl acetate/dichloromethane) to afford an oil (1.9 g). MS (+ve ion electrospray) m/e 253 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618959B2
Source datasetuspto-grants-2009_11
ORD IDord-7e40c1c1eb6b497e8956bab2d8bdc99f
Source noteuspto-grants-2009_11