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ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE

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ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Basic information

Product Name:
ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE
Synonyms:
  • ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE
  • 4-Hydroxy-5-pyrimidineacetic acid ethyl ester
  • 5-Pyrimidineaceticacid, 3,4-dihydro-4-oxo-, ethyl ester
  • ethyl 2-(6-oxo-1,6-dihydropyriMidin-5-yl)acetate
  • 2-(6-oxo-1H-pyrimidin-5-yl)acetic acid ethyl ester
  • ethyl 2-(6-oxo-1H-pyrimidin-5-yl)acetate
  • ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE ISO 9001:2015 REACH
CAS:
6214-46-6
MF:
C8H10N2O3
MW:
182.18
EINECS:
604-604-1
Product Categories:
  • Heterocycle-Pyrimidine series
Mol File:
6214-46-6.mol
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ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Chemical Properties

Melting point:
155-156 °C
Density 
1.27±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
8.62±0.40(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933599590
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ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Usage And Synthesis

Synthesis

3473-63-0

5472-38-8

6214-46-6

The ethanolic solution of sodium ethoxide was cooled to 0 °C under argon protection. Under continuous stirring, diethyl 2-formylsuccinate was slowly added. after 5 minutes, the corresponding formamidine acetate was added drop by drop while maintaining the condition of 0°C. Subsequently, the reaction mixture was warmed up to room temperature and stirred continuously for 3 days. After completion of the reaction, 5% aqueous hydrogen chloride solution was added and stirring was continued for 30 minutes. After addition of appropriate amount of water, ethanol was removed by distillation under reduced pressure at 30 °C. Finally, the precipitate was collected by filtration to afford the target product ethyl 4-hydroxy-5-pyrimidineacetate (Compound 1, where X = H, Me, Ph, SMe; Y = H, R1 = Et).

References

[1] Monatshefte fur Chemie, 2016, vol. 147, # 4, p. 767 - 773

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