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2-Chloro-4-methylpyridine-3-carbonitrile

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2-Chloro-4-methylpyridine-3-carbonitrile Basic information

Product Name:
2-Chloro-4-methylpyridine-3-carbonitrile
Synonyms:
  • 2-chloro-4-methyl-3-pyridinecarbonitrile
  • 2-Chloro-4-methylpyridine-3-carbonitrile
  • 2-chloro-4-methylnicotinonitrile
  • 2-Chloro-4-methyl-3-cyano-pyridine
  • 3-Pyridinecarbonitrile, 2-chloro-4-methyl-
  • 2-Chloro-4-methylpyridine-3-carbonitrile ISO 9001:2015 REACH
  • _x000D_2-Chloro-4-methylpyridine-3-carbonitrile
CAS:
65169-38-2
MF:
C7H5ClN2
MW:
152.58
Product Categories:
  • Boron, Nitrile, Thio,& TM-Cpds
  • Heterocycles
  • Pyridine
Mol File:
65169-38-2.mol
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2-Chloro-4-methylpyridine-3-carbonitrile Chemical Properties

Melting point:
108-109°
storage temp. 
Inert atmosphere,Room Temperature
form 
solid
color 
Light brown to brown
InChI
InChI=1S/C7H5ClN2/c1-5-2-3-10-7(8)6(5)4-9/h2-3H,1H3
InChIKey
BXUFVXSRHLSIMN-UHFFFAOYSA-N
SMILES
C1(Cl)=NC=CC(C)=C1C#N
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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2-Chloro-4-methylpyridine-3-carbonitrile Usage And Synthesis

Synthesis

93271-59-1

65169-38-2

General procedure for the synthesis of 2-chloro-3-cyano-4-methylpyridine from 3-cyano-4-methyl-2-pyridone: (c) Preparation of 2-chloro-3-cyano-4-methylpyridine (chlorination) 4-Methyl-3-cyano-2-pyridone (40.7 g, 0.304 mol) was added to a stirred mixed solution of phosphorus trichloride (POCL3, 140 g, 0.912 mol) and phosphorus pentachloride (PCl5, 19.0 g, 0.091 mol). The reaction mixture was heated to reflux (about 115 °C) and maintained at this temperature for 2 hours of reaction. Upon completion of the reaction, the excess phosphorous trichloride was removed by distillation. After the reaction mixture was cooled to room temperature, it was quenched by slowly adding water (30 mL). The aqueous phase was extracted with dichloromethane (30 mL), and the organic phases were combined and concentrated to give 43.2 g of a tan solid, which was identified as 2-chloro-3-cyano-4-methylpyridine (4). The melting point was 102-104 °C. The yield was 98.2%. 1H NMR (CDCl3): δ 8.03 (d, J = 2 Hz, 1H), 7.6 (d, J = 2 Hz, 1H), 2.5 (s, 3H). 13C NMR (CDCl3): δ 156.1, 152.6, 151.8, 124.9, 114.4, 111.8, 20.6; δ 156.1, 152.6, 151.8, 124.9, 114.4, 111.8, 20.6. FTIR (KBr, cm-1): 3144, 2979, 2834, 2228, 1653, 1616, 1540, 1484, 1242, 1218, 1173, 819, 607.

References

[1] Patent: US2002/52507, 2002, A1
[2] Patent: EP1679003, 2006, A1. Location in patent: Page/Page column 22

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