Basic information Safety Supplier Related

5-FLUOROPHTALIC ACID

Basic information Safety Supplier Related

5-FLUOROPHTALIC ACID Basic information

Product Name:
5-FLUOROPHTALIC ACID
Synonyms:
  • 5-FLUORO-ISOPHTHALIC ACID
  • 5-FLUOROPHTALIC ACID
  • Nsc302311
  • 5-Fluorobenzene-1,3-dicarboxylic acid
  • JACS-1583-66-0
  • 1,3-Benzenedicarboxylic acid, 5-fluoro-
CAS:
1583-66-0
MF:
C8H5FO4
MW:
184.12
Product Categories:
  • Fluorine series
Mol File:
1583-66-0.mol
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5-FLUOROPHTALIC ACID Chemical Properties

Melting point:
295-297℃
Boiling point:
407.7±30.0 °C(Predicted)
Density 
1.551
storage temp. 
Sealed in dry,Room Temperature
pka
3.19±0.10(Predicted)
form 
solid
color 
Off-white
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
2917399590
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5-FLUOROPHTALIC ACID Usage And Synthesis

Uses

5-Fluoroisophthalic Acid is a useful research chemical.

Synthesis

461-97-2

1583-66-0

General Steps: 1. 1.9 g (15.3 mmol) of 3,5-dimethylfluorobenzene was dissolved in a solvent mixture of about 13.5 mL of pyridine and about 9.5 mL of water under mild reflux conditions. 2. 13.8 g (87.3 mmol) of potassium permanganate (KMnO4) was added to the above solution in batches. 3. The reaction mixture was refluxed for about 7 hours to ensure complete reaction. 4. Upon completion of the reaction, an appropriate amount of sodium sulfite was added to quench the unreacted potassium permanganate. 5. Filter the reaction mixture while hot to remove insoluble impurities. 6. 6. To the filtrate, 1N hydrochloric acid (HCl) was slowly added to adjust the pH to 3. 7. 7. The filtrate was washed with ethyl acetate (EtOAc) and subsequently saturated with sodium chloride (NaCl). 8. The aqueous phase was extracted 3-4 times using a solvent mixture consisting of 80 mL of chloroform (CHCl3), 10 mL of methanol (MeOH) and 10 mL of water (H2O). 9. All organic extracts were combined and dried with anhydrous sodium sulfate. 10. The dried organic phase was filtered and the filtrate was concentrated to give about 400 mg (14% yield) of 5-fluoroisophthalic acid as a light yellow solid.

References

[1] Patent: WO2006/110668, 2006, A1. Location in patent: Page/Page column 55; 60
[2] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1984, # 3, p. 529 - 532
[3] Patent: US2003/181334, 2003, A1

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