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2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE

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2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE Basic information

Product Name:
2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE
Synonyms:
  • 4-Chloro-2-(trifluoromethyl)pyridine 99%
  • Pyridine,4-chloro-2-(trifluoromethyl)-
  • 2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE
  • 4-CHLORO-2-(TRIFLUOROMETHYL)PYRIDINE
  • 4-Chloro-2-(TrifluoroMeth
  • 4-Chloro-alpha,alpha,alpha-trifluoro-2-picoline
  • 2-Trifluoromethyl-4-Chloropyridine(WX636118)
  • 4-Chloro-2-(trifluoromethyl)pyridine,98%
CAS:
131748-14-6
MF:
C6H3ClF3N
MW:
181.54
EINECS:
1312995-182-4
Product Categories:
  • Fluorine series
  • alkyl chloride
Mol File:
131748-14-6.mol
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2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE Chemical Properties

Boiling point:
137.4±35.0 °C(Predicted)
Density 
1.417
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.29±0.10(Predicted)
form 
Liquid
color 
Colorless
Water Solubility 
Slightly soluble in water.
InChI
InChI=1S/C6H3ClF3N/c7-4-1-2-11-5(3-4)6(8,9)10/h1-3H
InChIKey
FZINIBTZNSPWQR-UHFFFAOYSA-N
SMILES
C1(C(F)(F)F)=NC=CC(Cl)=C1
CAS DataBase Reference
131748-14-6
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
25-36
Safety Statements 
26-45
RIDADR 
UN2811
HazardClass 
IRRITANT
HazardClass 
6.1
HS Code 
2933399990
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2-TRIFLUOROMETHYL-4-CHLOROPYRIDINE Usage And Synthesis

Uses

Chloro(trifluoromethyl)pyridines derivatives are used as model substrates for regioexhaustive functionalization.

Synthesis

170886-13-2

131748-14-6

Example 1 Preparation of 4-chloro-2-trifluoromethylpyridine: In a 25 mL round-bottomed flask equipped with a reflux condenser, a magnetic stirrer, and vented with inert gas, 1.63 g (10.0 mmol) of 2-trifluoromethyl-4-hydroxypyridine was dissolved in a solvent mixture of 4.9 mL of cyclohexane and 0.077 mL of DMF. At room temperature, 2.19 mL (25.0 mmol) oxalyl chloride was slowly added. The reaction mixture was heated to reflux for 3 hours and subsequently cooled to room temperature. 18 mL of water was added slowly and dropwise (watch for gas release), then the reaction mixture was extracted with 18 mL of methyl tert-butyl ether (MTBE). The organic layer was separated, washed with 1 M sodium bicarbonate (NaHCO3) solution and dried over anhydrous sodium sulfate (Na2SO4). After filtration, the solvent was evaporated under reduced pressure to give the crude product. The crude product was dissolved in 12 mL of hexane and stirred at room temperature for 5 min, filtered and evaporated under reduced pressure to give 0.9 g of 4-chloro-2-trifluoromethylpyridine as a yellow liquid. The product was analyzed by GC-EI-MS, showing molecular ion peaks at m/z 181 (M+) and m/z 183 (M+2).

References

[1] Patent: WO2017/221092, 2017, A1. Location in patent: Paragraph 00178
[2] Patent: WO2011/161612, 2011, A1. Location in patent: Page/Page column 13
[3] Patent: WO2014/76127, 2014, A1. Location in patent: Page/Page column 8
[4] Patent: WO2018/99812, 2018, A1. Location in patent: Page/Page column 70

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