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CHEMPACIFIC 38158

Basic information Safety Supplier Related

CHEMPACIFIC 38158 Basic information

Product Name:
CHEMPACIFIC 38158
Synonyms:
  • CHEMPACIFIC 38158
  • 2-CHLORO-6-CHLOROMETHYL-PYRIDINE
  • 6-CHLORO-2-CHLOROMETHYL-PYRIDINE
  • 2-chloro-6-(chloromethyl)pyridine(SALTDATA: FREE)
  • PYRIDINE, 2-CHLORO-6-(CHLOROMETHYL)-
  • 2-Chloro-6-(chloromethyl)
  • CHEMPACIFIC 38158 ISO 9001:2015 REACH
CAS:
78846-88-5
MF:
C6H5Cl2N
MW:
162.02
EINECS:
251-156-6
Mol File:
78846-88-5.mol
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CHEMPACIFIC 38158 Chemical Properties

Boiling point:
227.9±25.0 °C(Predicted)
Density 
1.324±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.06±0.10(Predicted)
form 
crystalline powder
color 
Beige
InChI
InChI=1S/C6H5Cl2N/c7-4-5-2-1-3-6(8)9-5/h1-3H,4H2
InChIKey
VHKDPJQJCMVQFZ-UHFFFAOYSA-N
SMILES
C1(Cl)=NC(CCl)=CC=C1
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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CHEMPACIFIC 38158 Usage And Synthesis

Synthesis

33674-97-4

78846-88-5

The general procedure for the synthesis of 2-chloro-6-(chloromethyl)pyridine from 2-chloro-6-hydroxymethylpyridine is as follows: Preparation of Example 52-1-2 2-chloro-6-(chloromethyl)pyridine: To a mixed solution containing (6-chloropyridin-2-yl)methanol (200 mg, 1.39 mmol) and toluene (3 mL), thionyl chloride (152 μL, 2.09 mmol) was slowly added under ice bath conditions. The reaction mixture was then stirred for 2 h at room temperature. Upon completion of the reaction, saturated aqueous sodium bicarbonate solution was added to the mixture to neutralize the excess thionyl chloride, followed by extraction with ethyl acetate. The organic layer was separated, washed sequentially with water and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (eluent: heptane/ethyl acetate=4:1) to afford the target product 2-chloro-6-(chloromethyl)pyridine (163.2 mg, 73% yield). 1H-NMR (CDCl3) δ (ppm): 4.64 (2H, s), 7.29 (1H, d, J=8.0 Hz), 7.44 (1H, d, J=7.6 Hz), 7.70 (1H, dd, J=7.6,8.0 Hz).

References

[1] Patent: US2009/82403, 2009, A1. Location in patent: Page/Page column 100
[2] Patent: US2007/105904, 2007, A1. Location in patent: Page/Page column 99-100
[3] Tetrahedron, 1982, vol. 38, # 22, p. 3277 - 3280
[4] Journal of Organic Chemistry, 2000, vol. 65, # 23, p. 7718 - 7722
[5] Journal of Organometallic Chemistry, 2002, vol. 650, # 1-2, p. 43 - 56

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