Basic information Safety Supplier Related

2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID

Basic information Safety Supplier Related

2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID Basic information

Product Name:
2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID
Synonyms:
  • (6-Hydroxybenzofuran-3-yl)acetic acid
  • 2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID, 97
  • 2-(6-Hydroxy-1-benzofuran-3-yl)aceticacid
  • 3-Benzofuranacetic acid, 6-hydroxy-
  • 2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID, 97-3
  • 6-Hydroxy-3-benzofuranacetic acid
CAS:
69716-04-7
MF:
C10H8O4
MW:
192.17
Mol File:
69716-04-7.mol
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2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID Chemical Properties

Melting point:
139-140℃
Boiling point:
251.5±9.0℃ (760 Torr)
Density 
1.453±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
105.9±18.7℃
storage temp. 
Sealed in dry,Room Temperature
pka
4.12±0.30(Predicted)
Appearance
White to light brown Solid
InChI
InChI=1S/C10H8O4/c11-7-1-2-8-6(3-10(12)13)5-14-9(8)4-7/h1-2,4-5,11H,3H2,(H,12,13)
InChIKey
ZEMXZWJZCWCPBM-UHFFFAOYSA-N
SMILES
O1C2=CC(O)=CC=C2C(CC(O)=O)=C1
CAS DataBase Reference
69716-04-7
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Safety Information

HS Code 
2932990090
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2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID Usage And Synthesis

Uses

(6-Hydroxy-1-benzofuran-3-yl)acetic Acid is a reactant in the synthesis of dihydrobenzofuran (6-{[4''-(2-ethoxyethoxy)-2'',6''-dimethylbiphenyl-3-yl]methoxy}-2,3-dihydro-1-benzofuran-3-yl)acetic acid as a potent and orally available GPR40/FFA1 agonist.

Synthesis

25392-41-0

69716-04-7

General procedure for the synthesis of 2-(6-hydroxybenzofuran-3-yl)acetic acid from 4-chloromethyl-7-hydroxychromen-2-one: 1. a mixture of 4-chloromethyl-7-hydroxychromen-2-one (21.0 g, 21.0 mmol) with 1 M aqueous sodium hydroxide solution (1 L) was stirred under reflux conditions for 2 hours. 2. After completion of the reaction, the reaction mixture was acidified with concentrated sulfuric acid. 3. The acidified mixture was extracted with ethyl acetate. 4. The extract was washed with saturated sodium chloride solution and dried over anhydrous sodium sulfate. 5. The dried organic phase was concentrated under pressure to give the intermediate (6-hydroxy-1-benzofuran-3-yl)acetic acid (18.0 g, 93.75% yield).

References

[1] Heterocycles, 1995, vol. 41, # 4, p. 647 - 650
[2] Patent: WO2012/11125, 2012, A1. Location in patent: Page/Page column 136-137
[3] Patent: WO2008/1931, 2008, A2. Location in patent: Page/Page column 87
[4] Journal of Medicinal Chemistry, 2012, vol. 55, # 4, p. 1538 - 1552
[5] Patent: CN104250239, 2016, B. Location in patent: Paragraph 0292; 0293; 0294

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