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

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Products Intro: Product Name:2-(6-Hydroxy-1-benzofuran-3-yl)aceticacid
CAS:69716-04-7
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2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID manufacturers

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
EINECS:
Product Categories:
Mol File:69716-04-7.mol
2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID Structure
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)
Fp 105.9±18.7℃
storage temp. Sealed in dry,Room Temperature
pka4.12±0.30(Predicted)
AppearanceWhite to light brown Solid
InChIInChI=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)
InChIKeyZEMXZWJZCWCPBM-UHFFFAOYSA-N
SMILESO1C2=CC(O)=CC=C2C(CC(O)=O)=C1
CAS DataBase Reference69716-04-7
Safety Information
HS Code 2932990090
MSDS Information
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
4-(CHLOROMETHYL)-7-HYDROXY-2H-CHROMEN-2-ONE

25392-41-0

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

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
Tag:2-(6-HYDROXY-1-BENZOFURAN-3-YL) ACETIC ACID(69716-04-7) Related Product Information
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