2-chloro-6-(trifluoroMethoxy)pyridine
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
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
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
2-chloro-6-(trifluoroMethoxy)pyridineSupplier
- Tel
- 029-86115547 17791676824
- sales@cochemical.com
- Tel
- 0512-85667806 18551283436
- sales@sanbem.com
- Tel
- 021-65170832 15601903708
- qinba_1@163.com
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 025-86918202 4000255188
- sales@pharmablock.com