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Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate

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Products Intro: Product Name:Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate
CAS:1174046-84-4
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Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate manufacturers

Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate Basic information
Product Name:Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate
Synonyms:Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate;3-Pyridinecarboxylic acid, 4-ethoxy-1,2-dihydro-2-oxo-, ethyl ester;thyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate;Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxyla;Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate ISO 9001:2015 REACH;ethyl 4-ethoxy-2-oxo-1H-pyridine-3-carboxylate;Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3
CAS:1174046-84-4
MF:C10H13NO4
MW:211.21
EINECS:
Product Categories:
Mol File:1174046-84-4.mol
Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate Structure
Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate Chemical Properties
Boiling point 424.6±45.0 °C(Predicted)
density 1.19±0.1 g/cm3 (20 ºC 760 Torr)
storage temp. Sealed in dry,Room Temperature
pka9.29±0.10(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
MSDS Information
Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate Usage And Synthesis
Synthesis
ethyl 2-cyano-5-(dimethylamino)-3-ethoxypenta-2,4-die

1345855-03-9

Ethyl 4-Ethoxy-2-oxo-1,2-dihydropyridine-3-carboxylate

1174046-84-4

General procedure for the synthesis of ethyl 2-oxo-4-ethoxy-1,2-dihydropyridine-3-carboxylate from ethyl 2-cyano-5-(dimethylamino)-3-ethoxypenta-2,4-dienoate: ethyl 2-cyano-5-(dimethylamino)-3-ethoxypenta-2,4-dienoate (15.0 g, 63 mmol) was mixed with acetic acid (600 mL) and reacted at reflux overnight. After completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove the solvent. The residue was treated with water and washed with ethyl acetate (2×). The aqueous layer was adjusted to pH 9-10 with sodium bicarbonate and extracted with dichloromethane (3×). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Finally, it was purified by silica gel column chromatography to afford ethyl 2-oxo-4-ethoxy-1,2-dihydropyridine-3-carboxylate (9.0 g, 67% yield).

References[1] Patent: WO2014/145004, 2014, A1. Location in patent: Paragraph 0103
[2] Patent: WO2011/139891, 2011, A1. Location in patent: Page/Page column 59
[3] Patent: WO2013/78295, 2013, A2. Location in patent: Paragraph 00184
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