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4-Bromo-1H-indole-7-carboxylic acid

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4-Bromo-1H-indole-7-carboxylic acid Basic information

Product Name:
4-Bromo-1H-indole-7-carboxylic acid
Synonyms:
  • 1H-Indole-7-carboxylic acid, 4-broMo-
  • 4-broMo-1H-indole-7-carboxylic acid
  • 4-Bromoindole-7-carboxylic Acid
CAS:
1211594-25-0
MF:
C9H6BrNO2
MW:
240.05
Mol File:
1211594-25-0.mol
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4-Bromo-1H-indole-7-carboxylic acid Chemical Properties

Boiling point:
455.8±30.0 °C(Predicted)
Density 
1.838±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
4.54±0.10(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C9H6BrNO2/c10-7-2-1-6(9(12)13)8-5(7)3-4-11-8/h1-4,11H,(H,12,13)
InChIKey
CDTILRQKJWYBOM-UHFFFAOYSA-N
SMILES
N1C2=C(C(Br)=CC=C2C(O)=O)C=C1
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4-Bromo-1H-indole-7-carboxylic acid Usage And Synthesis

Synthesis

1224724-39-3

1211594-25-0

To a solution of methyl 4-bromo-1H-indole-7-carboxylate (6 g, 23 mmol, Preparation 1 Step B) in tetrahydrofuran (THF, 300 mL) was added water (60 mL), methanol (MeOH, 60 mL) and lithium hydroxide (2.83 g, 118 mmol). The reaction mixture was heated to reflux and stirred overnight. After completion of the reaction, it was cooled to room temperature and concentrated under reduced pressure to remove the solvent. To the remaining aqueous layer 4N hydrochloric acid (HCl) was slowly added to adjust the pH to about 6. The precipitate precipitated was collected by filtration and the solid was dried to give 4-bromo-1H-indole-7-carboxylic acid (5.5 g, 97% yield). The structure of the product was confirmed by 1H NMR (DMSO-d6): δ 11.39 (br, 1H), 7.65-7.63 (d, J = 8.0 Hz, 1H), 7.46-7.44 (m, 1H), 7.33-7.31 (d, J = 8.0 Hz, 1H), 6.49-6.48 (m, 1H).

References

[1] Patent: WO2014/210255, 2014, A1. Location in patent: Page/Page column 101

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