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4,6-Dichloro-5-nitronicotinic acid ethyl ester

Basic information Safety Supplier Related

4,6-Dichloro-5-nitronicotinic acid ethyl ester Basic information

Product Name:
4,6-Dichloro-5-nitronicotinic acid ethyl ester
Synonyms:
  • 4,6-Dichloro-5-nitronicotinic acid ethyl ester
  • Ethyl 4,6-dichloro-5-nitronicotinate
  • Ethyl 4,6-dichloro-5-nitropyridine-3-carboxylate, 2,4-Dichloro-5-(ethoxycarbonyl)-3-nitropyridine
  • 3-Pyridinecarboxylic acid, 4,6-dichloro-5-nitro-, ethyl ester
  • ethyl 4,6-dichloro-5-nitro-pyridine-3-carboxylate
CAS:
154012-15-4
MF:
C8H6Cl2N2O4
MW:
265.05
EINECS:
604-604-1
Mol File:
154012-15-4.mol
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4,6-Dichloro-5-nitronicotinic acid ethyl ester Chemical Properties

Melting point:
36-38°
Boiling point:
352.9±37.0 °C(Predicted)
Density 
1.533±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-3.86±0.10(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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4,6-Dichloro-5-nitronicotinic acid ethyl ester Usage And Synthesis

Synthesis

6317-97-1

154012-15-4

Step 3: Preparation of ethyl 4,6-dichloro-5-nitronicotinate (16) Ethyl 4,6-dihydroxy-5-nitronicotinate (15) (20.0 g, 87.7 mmol) was dissolved in phosphoryl chloride (80 mL, 874 mmol). The reaction mixture was stirred at 80 °C for 24 hours. Upon completion of the reaction, about half the volume of phosphoryl chloride was evaporated under reduced pressure. The residue was slowly poured into ice water and extracted twice with ethyl acetate. The organic phases were combined and washed sequentially with aqueous sodium carbonate, water and saturated saline. The organic layers were dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give a brown oily crude product. The crude product was purified by silica gel column chromatography with petroleum ether/ethyl acetate (3:1, v/v) as eluent to give white crystalline solid 16 (14.2 g, yield 61.1%). The melting point of the product was 36-38 °C. 1H NMR (300 MHz, DMSO-d6) δ: 9.07 (s, 1H), 4.39 (q, J = 6.0 Hz, 2H), 1.34 (t, J = 6.0 Hz, 3H). m/z MS (ESI (+) 70 V): 264 [M + H]+.

References

[1] Journal of Heterocyclic Chemistry, 1993, vol. 30, # 4, p. 855 - 859
[2] Patent: WO2008/17696, 2008, A1. Location in patent: Page/Page column 51
[3] Patent: WO2009/106419, 2009, A1. Location in patent: Page/Page column 79
[4] Patent: WO2008/17696, 2008, A1. Location in patent: Page/Page column 51
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 20, p. 6551 - 6559

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