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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387795Generated: October 30, 2026

Acetone → Ethyl(E)-3-[2-amino-4-(4-nitrophenoxy)-3-pyridyl]-2-propenoate

https://huagongshe.com/reaction/387795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantTributylamineHCID 7622—
ReactantEthyl AcrylateHCID 8821—
Reactant3-Iodo-4-(4-nitrophenoxy)-2-pyridinamineHCID 22936334—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
ProductEthyl(E)-3-[2-amino-4-(4-nitrophenoxy)-3-pyridyl]-2-propenoateHCID 58931221—

Reaction Steps

3-Iodo-4-(4-nitrophenoxy)-2-pyridineamine (500 mg), ethyl acrylate (0.3 ml), palladium (II) acetate (30 mg), tributylamine (0.66 ml) and dimethylformaldehyde (5 ml) were stirred at 130° C. for 20 minutes. After returning the reaction solution to room temperature, water was added and extraction was performed with ethyl acetate. NH type silica gel was added to the extract, the solvent was distilled off under reduced pressure, and the reaction product was adsorbed onto the silica gel. The silica gel was charged into a dry column packed with NH type silica gel, and column purification was performed (hexane:ethyl acetate=3:1). The solvent was distilled off under reduced pressure to obtain 330 mg of the target substance as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372981B2
Source datasetuspto-grants-2013_02
ORD IDord-f92ef3996e974631b8f8793a5b7f8d77
Source noteuspto-grants-2013_02