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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 99%;5-Carboxy-2-iodobenzotrifluoride;4-Iodo-3-(trifluoromethyl)benzoicacid99%;Benzoic acid, 4-iodo-3-(trifluoromethyl)-;4-Iodo-3-(trifluoromethyl)benzoic acid
CAS:914636-20-7
MF:C8H4F3IO2
MW:316.02
EINECS:
Product Categories:
Mol File:Mol File
4-Iodo-3-(trifluoromethyl)benzoic acid Structure
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
pka3.59±0.10(Predicted)
form crystalline needles
color Tan/brown
Sensitive Light Sensitive/Air Sensitive
Safety Information
Hazard Codes Xi
HS Code 2916399090
MSDS Information
4-Iodo-3-(trifluoromethyl)benzoic acid Usage And Synthesis
Synthesis
4-Amino-3-(Trifluoromethyl)Benzoic Acid 3-Trifluoromethyl-4-Aminobenzoic Acid

400-76-0

4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID

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
4-Iodo-3-(trifluoromethyl)benzoic acid Preparation Products And Raw materials
Raw materialsSodium nitrite-->4-Amino-3-(Trifluoromethyl)Benzoic Acid 3-Trifluoromethyl-4-Aminobenzoic Acid-->Potassium iodide-->Hydrochloric acid
Tag:4-Iodo-3-(trifluoromethyl)benzoic acid(914636-20-7) Related Product Information
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