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2-Trifluoromethyl-6-pyridinecarboxylic acid

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2-Trifluoromethyl-6-pyridinecarboxylic acid Basic information

Product Name:
2-Trifluoromethyl-6-pyridinecarboxylic acid
Synonyms:
  • 2-TRIFLUOROMETHYL-6-PYRIDINECARBOXYLIC ACID
  • 6-(TRIFLUOROMETHYL)PICOLINIC ACID
  • 6-TRIFLUOROMETHYLPYRIDINE-2-CARBOXYLIC ACID
  • 6-(Trifluoromethyl)pyridine-2-carboxylic acid 97%
  • 6-(Trifluoromethyl)pyridine-2-carboxylicacid97%
  • 6-(Trifluoromethyl)picolinic acid, 2-Carboxy-6-(trifluoromethyl)pyridine
  • 6-TrifluoroMethyl-2-pyridinecarboxylic acid
  • 6-(trifluoroMethyl)pyridin-2-carboxylic acid
CAS:
131747-42-7
MF:
C7H4F3NO2
MW:
191.11
Product Categories:
  • Building Blocks
  • C7 to C8
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • New Products for Chemical Synthesis
  • Carboxylic Acids
  • Pyridine series
  • Carboxylic Acids
  • Pyridines
Mol File:
131747-42-7.mol
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2-Trifluoromethyl-6-pyridinecarboxylic acid Chemical Properties

Melting point:
154-158 °C
Boiling point:
263.0±40.0 °C(Predicted)
Density 
1.484±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Solid
pka
3.21±0.10(Predicted)
color 
Off-white
InChI
InChI=1S/C7H4F3NO2/c8-7(9,10)5-3-1-2-4(11-5)6(12)13/h1-3H,(H,12,13)
InChIKey
OKBHXGBLXDNJJD-UHFFFAOYSA-N
SMILES
C1(C(O)=O)=NC(C(F)(F)F)=CC=C1
CAS DataBase Reference
131747-42-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-36/37/38
Safety Statements 
26
RIDADR 
UN2811
WGK Germany 
3
HazardClass 
IRRITANT
HazardClass 
6.1
HS Code 
2933399990
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2-Trifluoromethyl-6-pyridinecarboxylic acid Usage And Synthesis

Chemical Properties

White powder

Uses

A useful organic intermediate.

Synthesis

124-38-9

189278-27-1

131747-42-7

General procedure for the synthesis of 6-(trifluoromethyl)pyridine-2-carboxylic acid from carbon dioxide and 2-bromo-6-trifluoromethylpyridine: 1. 2-Bromo-6-(trifluoromethyl)pyridine (100 mg, 0.44 mmol, 1 eq.) was dissolved in anhydrous ether at room temperature and protected by nitrogen and subsequently cooled to -70 °C. 2. 1.6 M hexane solution of n-butyllithium (0.28 mL, 0.44 mmol, 1 eq.) was added slowly and dropwise through the addition funnel. 3. The reaction mixture was stirred at -40 °C for 15 minutes and then cooled to -70 °C again. 4. Carbon dioxide gas was introduced into the reaction mixture and continuously bubbled for 10 minutes. 5. Allow the reaction mixture to warm slowly to room temperature. 6. 6. the reaction was terminated by addition of water and subsequently washed three times with ether. 7. Adjust the pH of the aqueous layer to 3 with concentrated hydrochloric acid. 8. Extracted the acidic aqueous layer with ethyl acetate three times. 9. The ethyl acetate layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give 6-(trifluoromethyl)pyridine-2-carboxylic acid (30 mg) as a white solid in 35% yield. 10. The product was detected by LCMS and the molecular ion peak (M + H)+ = 192.06 was confirmed.

References

[1] European Journal of Organic Chemistry, 2003, # 8, p. 1559 - 1568
[2] Patent: US2005/54626, 2005, A1. Location in patent: Page/Page column 36

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