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4-Benzofurancarboxylic Acid

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4-Benzofurancarboxylic Acid Basic information

Product Name:
4-Benzofurancarboxylic Acid
Synonyms:
  • benzofuran-4-carboxylic acid
  • 4-BENZOFURANCARBOXYLICACID
  • 1-Benzofuran-4-carboxylic acid
  • 1-benzofurane-4-carboxylic acid
  • 1-benzofuran-4-carboxylicaci
  • 4-Benzofurancarboxylic Acid ISO 9001:2015 REACH
  • Degarelix Impurity 1
CAS:
166599-84-4
MF:
C9H6O3
MW:
162.14
Mol File:
166599-84-4.mol
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4-Benzofurancarboxylic Acid Chemical Properties

Boiling point:
326℃
Density 
1.363
Flash point:
151℃
storage temp. 
Sealed in dry,Room Temperature
pka
3.19±0.10(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C9H6O3/c10-9(11)7-2-1-3-8-6(7)4-5-12-8/h1-5H,(H,10,11)
InChIKey
WFAPIZKLEVLUMX-UHFFFAOYSA-N
SMILES
O1C2=CC=CC(C(O)=O)=C2C=C1
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4-Benzofurancarboxylic Acid Usage And Synthesis

Uses

4-Benzofurancarboxylic Acid is a benzofuran derivative used in the preparation of dual orexin 1 and orexin 2 receptor antagonist which are useful for the treatment of sleep disorders.

Synthesis

41019-56-1

166599-84-4

General procedure for the synthesis of benzofuran-4-carboxylic acid from methyl benzofuran-4-carboxylate: a solution of LiOH (1.44 g, 34.3 mmol) in water (20 mL) was added to a mixture of THF (20 mL) and MeOH (20 mL) of methyl benzofuran-4-carboxylate (2.02 g, 11.4 mmol) and the reaction was stirred at room temperature for 16 The reaction was stirred for 16 hours at room temperature. After completion of the reaction, the solvent was removed by evaporation. The residue was dissolved in water (50 mL) and acidified with concentrated HCl to pH < 2. The precipitate was collected by filtration and dried to afford benzofuran-4-carboxylic acid (1.83 g, 99% yield). The product was characterized by 1H NMR (DMSO-d6): δ 13.10 (s, 1H), 8.14 (d, J = 2.1 Hz, 1H), 7.85-7.91 (m, 2H), 7.43 (t, J = 7.9 Hz, 1H), 7.33 (dd, J = 2.1, 1.0 Hz, 1H). Mass spectrum measured value: [M-H]? = 161.1.

References

[1] Patent: WO2017/155909, 2017, A1. Location in patent: Paragraph 0190
[2] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 8, p. 1797 - 1809
[3] Journal of Medicinal Chemistry, 1995, vol. 38, # 16, p. 3094 - 3105

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