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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271678Generated: November 2, 2026

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

https://huagongshe.com/reaction/1271678

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-nitro-benzaldehyde (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 ether, and the ether layer was washed with 0.5M sodium hydroxide, dried over anhydrous sodium sulphate and evaporated to give an oil that was chromatographed on silica gel (ethyl acetate/dichloromethane) to afford an oil (1.9 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205408B2
Source datasetuspto-grants-2007_04
ORD IDord-e9fa6cc2bdd7468d91bb4821e6668ea7
Source noteuspto-grants-2007_04