Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Pyridine derivatives >  5-(Trifluoromethyl)nicotinic acid

5-(Trifluoromethyl)nicotinic acid

Basic information Safety Supplier Related

5-(Trifluoromethyl)nicotinic acid Basic information

Product Name:
5-(Trifluoromethyl)nicotinic acid
Synonyms:
  • 5-TRIFLUOROMETHYLINICOTINIC ACID
  • 5-(Trifluoromethyl)-3-pyridinecarboxylic acid
  • 5-(TRIFLUOROMETHYL)NICOTINIC ACID
  • 5-(TRIFLUOROMETHYL)PYRIDINE-3-CARBOXYLIC ACID
  • 5-(Trifluoromethy)pyridine-3-carboxylic acid
  • 5-(trifluoroMethyl)pyridin-3-carboxylic acid
  • 5-(Trifluoromethyl)pyridine-3-carboxylic acid, 3-Carboxy-5-(trifluoromethyl)pyridine
  • 5-(TrifluoroMethyl)pyridine-3-carboxylic acid
CAS:
131747-40-5
MF:
C7H4F3NO2
MW:
191.11
Product Categories:
  • Carboxylic Acids
  • Pyridines
  • Carboxylic Acids
Mol File:
131747-40-5.mol
More
Less

5-(Trifluoromethyl)nicotinic acid Chemical Properties

Melting point:
184-189℃
Boiling point:
277.5±40.0 °C(Predicted)
Density 
1.484±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
Solid
pka
3.04±0.10(Predicted)
color 
Off-white
More
Less

Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
RIDADR 
UN2811
WGK Germany 
3
HazardClass 
IRRITANT
HazardClass 
6.1
HS Code 
2933399990
More
Less

5-(Trifluoromethyl)nicotinic acid Usage And Synthesis

Synthesis

124-38-9

436799-33-6

131747-40-5

The general procedure for synthesizing 5-trifluoromethylnicotinic acid from carbon dioxide and 3-bromo-5-(trifluoromethyl)pyridine is as follows: 1. 1.5 g of 3-bromo-5-(trifluoromethyl)pyridine was dissolved in 50 mL of toluene at -75 °C to prepare a solution. 2. the above solution was slowly added dropwise to a mixed system containing 9.96mL (15.9mmol) 1.6M butyl lithium hexane solution and 3.98mL (8mmol) 2M butyl magnesium chloride ethyl ether solution and 10mL THF. 3. After the dropwise addition was completed, the reaction system was kept at -75°C and continued to be stirred for 20 minutes. 4. Subsequently, 20 g (454 mmol) of dry ice was added to the reaction system and stirring was continued at -75°C for 20 minutes, then brought to room temperature and stirred for 3 hours. 5. Upon completion of the reaction, the reaction mixture was combined with 50 mL of 1 M sodium hydroxide solution and extracted twice with ether. 6. The aqueous phase was acidified to acidity with 4M hydrochloric acid and extracted with ether three times. 7. All organic phases were combined and dried with anhydrous sodium sulfate and subsequently evaporated to dryness under vacuum. 8. The residue was mixed with dichloromethane and the precipitate formed was collected by filtration. 9. Finally, the precipitate was placed in a circulating air dryer and dried at 55 °C to give the target product 5-trifluoromethylnicotinic acid. Yield: 9% based on the theoretical value of C7H4F3NO2 (191.11).

References

[1] European Journal of Organic Chemistry, 2003, # 8, p. 1559 - 1568
[2] Patent: US2010/240669, 2010, A1. Location in patent: Page/Page column 141

5-(Trifluoromethyl)nicotinic acidSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18934348241
Email
sales4.gd@hwrkchemical.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com