Basic information Safety Supplier Related

2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE

Basic information Safety Supplier Related

2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE Basic information

Product Name:
2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE
Synonyms:
  • 2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE
  • 3-Pyridinecarbonitrile, 2-chloro-4-(dimethylamino)-
  • 1-(Methoxymethyl)-5-(trifluoromethoxy)benzene
CAS:
147992-80-1
MF:
C8H8ClN3
MW:
181.62
Mol File:
147992-80-1.mol
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2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE Chemical Properties

Melting point:
84-86°
Boiling point:
343.4±42.0 °C(Predicted)
Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
1.71±0.10(Predicted)
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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2-CHLORO-4-(DIMETHYLAMINO)NICOTINONITRILE Usage And Synthesis

Synthesis

98694-71-4

147992-80-1

A slurry was prepared from 2-(1,3-bisdimethylamino-allyl)malononitrile (120.0 g, 632 mmol) in methanol (1500 mL). HCl gas was slowly passed at 0 °C and the reaction mixture became homogeneous after about 1 hour. Stirring was maintained at 0 °C and continued for 9 h under continuous passage of HCl gas. Subsequently, N2 was bubbled through the reaction mixture for 2 hours to remove residual HCl and then evaporated to remove all solvent. The residual solid was redissolved in CH2Cl2 and washed sequentially with water, aqueous K2C2O3 and water. The organic layer was separated and dried with Na2SO4. After filtration to remove the desiccant, the solvent was evaporated under reduced pressure to give the pure product 2-chloro-4-(dimethylamino)nicotinonitrile (113.0 g, 98% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 7.96 ppm (d, J=6.4 Hz, 1H); 6.59 (d, J=6.4 Hz, 1H); 3.30 (s, 6H). Mass spectrum (ESI, M+1): 181.9.

References

[1] Patent: WO2006/81072, 2006, A1. Location in patent: Page/Page column 30-31

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