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4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID

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4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID Basic information

Product Name:
4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID
Synonyms:
  • 4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID
  • 4-Iodo-3-(trifluoromethyl)benzoic acid 99%
  • 5-Carboxy-2-iodobenzotrifluoride
  • 4-Iodo-3-(trifluoromethyl)benzoicacid99%
  • Benzoic acid, 4-iodo-3-(trifluoromethyl)-
CAS:
914636-20-7
MF:
C8H4F3IO2
MW:
316.02
Mol File:
Mol File
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4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID Chemical Properties

Boiling point:
311.7±42.0 °C(Predicted)
Density 
2.005±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.59±0.10(Predicted)
form 
crystalline needles
color 
Tan/brown
Sensitive 
Light Sensitive/Air Sensitive
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Safety Information

Hazard Codes 
Xi
HS Code 
2916399090
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4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID Usage And Synthesis

Synthesis

400-76-0

914636-20-7

General procedure for the synthesis of 4-iodo-3-(trifluoromethyl)benzoic acid from 3-trifluoromethyl-4-aminobenzoic acid: 4-amino-3-trifluoromethylbenzoic acid (1.8 g, 8.8 mmol) was suspended in 30 mL of hydrochloric acid. An aqueous solution (15 mL) of sodium nitrite (0.76 g, 11.0 mmol) was slowly added dropwise at 0°C. The reaction mixture was stirred at 0-10 °C for 30 min. Subsequently, an aqueous solution (25 mL) of potassium iodide (14.6 g, 88 mmol) was added dropwise. The mixture was stirred at room temperature for 1 hour. After completion of the reaction, the product was extracted with ethyl acetate (80 mL) and the organic layer was washed with brine (80 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by fast chromatography using a gradient elution with ethyl acetate/hexane, resulting in 4-iodo-3-(trifluoromethyl)benzoic acid (2.4 g, 86% yield) as a solid.LC-ES/MS analysis showed m/e 339.3 (M+23) and 315.0 (M-1).

References

[1] Patent: WO2007/140174, 2007, A2. Location in patent: Page/Page column 42

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