Basic information Safety Supplier Related

2-chloro-6-(trifluoroMethoxy)pyridine

Basic information Safety Supplier Related

2-chloro-6-(trifluoroMethoxy)pyridine Basic information

Product Name:
2-chloro-6-(trifluoroMethoxy)pyridine
Synonyms:
  • 2-chloro-6-(trifluoroMethoxy)pyridine
  • Pyridine, 2-chloro-6-(trifluoromethoxy)-
CAS:
1221171-70-5
MF:
C6H3ClF3NO
MW:
197.54
Mol File:
1221171-70-5.mol
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2-chloro-6-(trifluoroMethoxy)pyridine Chemical Properties

Boiling point:
42-44 °C(Press: 15 Torr)
Density 
1.463±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
-3.87±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
InChI
InChI=1S/C6H3ClF3NO/c7-4-2-1-3-5(11-4)12-6(8,9)10/h1-3H
InChIKey
GZFNUCAMADABAO-UHFFFAOYSA-N
SMILES
C1(Cl)=NC(OC(F)(F)F)=CC=C1
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Safety Information

HS Code 
2933399990
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2-chloro-6-(trifluoroMethoxy)pyridine Usage And Synthesis

Uses

2-Chloro-6-(trifluoromethoxy)pyridine is used in the synthesis of anti-HCV agents.

Synthesis

1221171-69-2

1221171-70-5

(b) Synthesis of 2-chloro-6-(trifluoromethoxy)pyridine (1-5): a mixture of SbF3 (29.87 g, 167.10 mmol, 2 eq.) and SbCl5 (1.61 mL, 12.53 mmol, 0.15 eq.) was stirred at 120 °C under argon protection. Subsequently, 2-chloro-6-(trichloromethoxy)pyridine (20.63 g, 83.55 mmol, 1 eq.) was added slowly and dropwise over 20 min. The reaction mixture was continued to be stirred at 120 °C for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and diluted with the addition of dichloromethane (350 mL), followed by the addition of saturated sodium carbonate solution (350 mL) and 20% KF aqueous solution (175 mL) sequentially. The resulting biphasic mixture was filtered through Celite. The organic and aqueous layers were separated and the aqueous layer was extracted repeatedly with dichloromethane (5 x 100 mL). All organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated to dryness. The crude product was purified by vacuum distillation (pressure = 35 mbar, temperature = 81-83 °C) to afford 2-chloro-6-(trifluoromethoxy)pyridine as a colorless oil in 62% yield.1H NMR (CDCl3) δ (ppm): 6.96 (d, 1H), 7.27 (d, 1H), 7.75 (t, 1H).

References

[1] Patent: WO2012/93174, 2012, A1. Location in patent: Page/Page column 38
[2] Patent: WO2010/40461, 2010, A1. Location in patent: Page/Page column 17-18
[3] European Journal of Organic Chemistry, 2010, # 31, p. 6043 - 6066
[4] ChemMedChem, 2015, vol. 10, # 4, p. 715 - 726
[5] Journal of Fluorine Chemistry, 2017, vol. 203, p. 155 - 165

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