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6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID

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6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID Basic information

Product Name:
6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID
Synonyms:
  • 6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID
  • RARECHEM AL BE 0955
  • Indole-3-carboxylic acid, 6-fluoro-
  • OTAVA-BB 1149596
  • UKRORGSYN-BB BBV-5127372
  • 6-Fluoro-indole-3-carboxylic acid
  • 1H-Indole-3-carboxylic acid, 6-fluoro-
CAS:
23077-44-3
MF:
C9H6FNO2
MW:
179.15
Product Categories:
  • pharmacetical
Mol File:
23077-44-3.mol
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6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID Chemical Properties

Melting point:
242-244 °C (decomp)
Boiling point:
422.2±25.0 °C(Predicted)
Density 
1.510±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
3.73±0.10(Predicted)
Appearance
Off-white to light yellow Solid
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Safety Information

RIDADR 
UN2811
HS Code 
2933998090
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6-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID Usage And Synthesis

Synthesis

399-51-9

407-25-0

23077-44-3

Trifluoroacetic anhydride (9.009 mL, 64.8 mmol, 2.2 eq.) was added slowly and dropwise to a stirred solution of 6-fluoroindole (4.000 g, 29.6 mmol, 1.0 eq.) dissolved in DMF (25 mL) at 0 °C (temperature controlled using an external ice bath). After the reaction mixture was kept in the ice bath for 3 h, the reaction was quenched with 40 mL of 2N sodium carbonate solution. The precipitate was collected by filtration and washed with distilled water. The resulting solid was dissolved in 4 M NaOH solution (50 mL) and refluxed for 4 hours. After completion of the reaction, the mixture was cooled to room temperature and poured into 50 mL of distilled water. The mixture was cooled again in an ice bath and the pH was adjusted slowly by adding 6N HCl to 3. The precipitate precipitated was collected by filtration, washed with distilled water and dried under vacuum to give the off-white solid product 6-fluoro-1H-indole-3-carboxylic acid (3.5 g, 66% yield).

References

[1] Patent: WO2017/197177, 2017, A1. Location in patent: Paragraph 0219-0221
[2] ChemMedChem, 2012, vol. 7, # 11, p. 1915 - 1920

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