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5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER

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5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
  • METHYL-5-CYANOPYRIDINE-3-CARBOXYLATE
  • Methyl 5-cyano-pyridin-3-carboxylate
  • 5-Cyanonicotinic acid methyl ester
  • 3-Pyridinecarboxylic acid, 5-cyano-, methyl ester
  • 5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER ISO 9001:2015 REACH
  • Methyl 5-cyano-3-pyridinecarboxylate
CAS:
106726-82-3
MF:
C8H6N2O2
MW:
162.15
EINECS:
125-856-9
Product Categories:
  • Pyridine series
Mol File:
106726-82-3.mol
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5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Chemical Properties

Boiling point:
269.2±25.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
-0.25±0.20(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933399990
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5-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Synthesis

29681-44-5

544-92-3

106726-82-3

The general procedure for the synthesis of methyl 5-cyano-3-pyridinecarboxylate from methyl 5-bromonicotinate and cuprous cyanide was as follows: methyl 5-bromonicotinate (2.16 g, 10.0 mmol, 1.0 eq.) and cuprous(I) cyanide (1.79 g, 20.0 mmol, 2.0 eq.) were dissolved in anhydrous DMF (10 mL), and the reaction was carried out at reflux for 15 hours. Upon completion of the reaction, it was cooled to room temperature and the reaction mixture was filtered through a diatomaceous earth pad and rinsed with ethyl acetate (100 mL). Formation of a black precipitate was observed in the filtrate. Subsequently, the filtrate was washed with saturated saline (3 x 100 mL). The organic layer was dried with anhydrous sodium sulfate and concentrated by rotary evaporation at 40 °C to give 546 mg (33.7% yield) of light yellow solid product. The crude product was further purified by silica gel column chromatography (column size: 80 mm in diameter × 20 mm in height) with an eluent of 20-35% ethyl acetate/hexane mixture, resulting in 501 mg (30.9% yield) of methyl 5-cyano-3-pyridinecarboxylate as an off-white solid. Mass spectrometry result: m/e 163.07 ([M+H]+).

References

[1] Patent: WO2005/66126, 2005, A1. Location in patent: Page/Page column 66

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