Basic information Safety Supplier Related

3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID

Basic information Safety Supplier Related

3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Basic information

Product Name:
3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
Synonyms:
  • 3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID
  • 3'-(TRIFLUOROMETHYL)-1,1'-BIPHENYL-4-CARBOXYLIC ACID
  • AKOS BAR-0024
  • [1,1'-BIPHENYL]-4-CARBOXYLIC ACID, 3'-(TRIFLUOROMETHYL)-
  • RARECHEM AL BE 1367
  • 4-(3-(Trifluoromethyl)phenyl)benzoic acid
  • 4-[3-(trifluoromethyl)phenyl]benzoate
  • 3'-(Trifluoromethyl)[1,1'-biphenyl]-4-carboxylic acid
CAS:
195457-70-6
MF:
C14H9F3O2
MW:
266.22
Product Categories:
  • pharmacetical
Mol File:
195457-70-6.mol
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3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
Yellow
CAS DataBase Reference
195457-70-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2916399090
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3'-TRIFLUOROMETHYLBIPHENYL-4-CARBOXYLIC ACID Usage And Synthesis

Uses

4-(3-Trifluoromethylphenyl)benzoic Acid is a reagent used in the synthesis of aryl-substituted aspartic acid and diaminopropionic acid derivatives as inhibitors of glutamate transporter EAAT-2 (Excitatory amino acid transporters 2).

Synthesis

586-76-5

1423-26-3

195457-70-6

The general procedure for the synthesis of 4-(3-trifluoromethylphenyl)benzoic acid from 4-bromobenzoic acid and 3-(trifluoromethyl)phenylboronic acid was as follows: Pd(dppf)Cl2 (1.49 mmol, 1.09 g) was added to a mixture containing 4-bromobenzoic acid (14.9 mmol, 3.0 g), 3-(trifluoromethyl)phenylboronic acid (17.9 mmol, 3.4 g), and Cs2CO3 (37.3 mmol, 12.2 g) in a suspension with the solvent being a mixture of 30 mL dioxane and 7.5 mL ethanol. The reaction mixture was stirred at 80 °C for 2 hours. After completion of the reaction, it was cooled to room temperature, the solid product was collected by filtration and washed with methanol. The filtrate was concentrated and the residue was partitioned between ethyl acetate and 1N aqueous hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. To the concentrated residue was added dichloromethane, the resulting solid was collected by filtration, washed with dichloromethane and dried to give 4-(3-trifluoromethylphenyl)benzoic acid (3.58 g, 86% yield), which could be used in the next reaction without further purification.

References

[1] Patent: US2013/102584, 2013, A1. Location in patent: Paragraph 0307; 0308
[2] Journal of Medicinal Chemistry, 1997, vol. 40, # 20, p. 3144 - 3150

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