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2,6-dihydroxy-3-cyanopyridine

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2,6-dihydroxy-3-cyanopyridine Basic information

Product Name:
2,6-dihydroxy-3-cyanopyridine
Synonyms:
  • 2,6-dihydroxy-3-cyanopyridine
  • 3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-2-oxo-
  • 1,2-Dihydro-6-hydroxy-2-oxo-3-pyridinecarbonitrile
  • 2-hydroxy-6-oxo-1,6-dihydropyridine-3-carbonitrile
  • 2,6-dihydroxynicotinonitrile
  • 2-hydroxy-6-oxo-1H-pyridine-3-carbonitrile
  • 2,6-dihydroxy-3-cyanopyridine ISO 9001:2015 REACH
  • 6-Hydroxy-2-oxo-1,2-dihydropyridine-3-carbonitrile
CAS:
35441-10-2
MF:
C6H4N2O2
MW:
136.11
Mol File:
35441-10-2.mol
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2,6-dihydroxy-3-cyanopyridine Chemical Properties

Melting point:
255 °C(Solv: ethanol (64-17-5))
Boiling point:
349.9±42.0 °C(Predicted)
Density 
1.47±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
pka
3.51±0.58(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

HS Code 
2933399990
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2,6-dihydroxy-3-cyanopyridine Usage And Synthesis

Synthesis

91467-46-8

35441-10-2

In a 2000 L reaction flask, 160 g of 1,3-dibenzyluracil, 55.2 g of cyanoacetamide (1.2 eq.) and sodium methanol were added. Subsequently 2556.6 g (2.5 eq.) of liquid and 800 mL of methanol were added and stirring was initiated. The temperature of the reaction system was raised to 45-50 °C and the reaction was maintained at this temperature for 6 hours. The progress of the reaction was monitored by TLC and after confirming the completion of the reaction, the reaction solution was cooled to 20-30 °C, filtered and the filter cake was washed with 100 mL of methanol. The filter cake was transferred to a 2000 L reaction flask along with 800 g of water. After heating to 70-75 °C, the reaction solution was slowly cooled to 0-5 °C and kept at this temperature for 2 h. Subsequently, filtration was performed and the filter cake was washed with an appropriate amount of ice water to obtain 2,6-dihydroxynicotinonitrile monosodium salt dihydrate. The temperature was controlled at 20-30 °C and the filter cake was slowly added to an aqueous hydrochloric acid solution (prepared from 480 g of water and 66.6 g of concentrated hydrochloric acid). The crystallization was held at 20-30 °C for 1 h. The crystallization was continued to be cooled to 0-5 °C and kept for 2 h. The filtration was withdrawn and the filter cake was washed with an appropriate amount of ice water. After drying, 74.5 g of white solid 3-cyano-2,6-dihydroxypyridine was obtained in 86.5% yield. Its 1H NMR spectrum is shown in Figure 6.

References

[1] Patent: CN108341771, 2018, A. Location in patent: Paragraph 0056-0061

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