5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID
CAS:56172-36-2
Purity:NLT 98% Package:1G;1KG;100KG
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:5-Hydroxybenzofuran-2-carboxylic acid
CAS:56172-36-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-24360
Company Name: Hefei TNJ Chemical Industry Co.,Ltd.
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Products Intro: Product Name:2-Benzofurancarboxylic acid, 5-hydroxy-
CAS:56172-36-2
Company Name: Coresyn Pharmatech Co., Ltd.
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Products Intro: Product Name:5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID
CAS:56172-36-2
Purity:NLT 98% Package:1G;1KG;100KG Remarks:CF12030
Company Name: Amadis Chemical Company Limited
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Products Intro: Product Name:5-hydroxy-2-Benzofurancarboxylic acid
CAS:56172-36-2
Purity:0.97 Package:mgs,gs,kgs Remarks:A870002
5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Basic information
Product Name:5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID
Synonyms:5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID;5-HYDROXY-BENZOFURAN-2-CARBOXYLIC ACID;5-hydroxy-2-Benzofurancarboxylic acid;2-Benzofurancarboxylic acid, 5-hydroxy-
CAS:56172-36-2
MF:C9H6O4
MW:178.14
EINECS:
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Mol File:56172-36-2.mol
5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Structure
5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Chemical Properties
Melting point 252-254 °C
Boiling point 396.4±22.0 °C(Predicted)
density 1.518±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
pka3.06±0.30(Predicted)
Safety Information
MSDS Information
5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Usage And Synthesis
Synthesis
5-Methoxybenzofuran-2-carboxylic acid

10242-08-7

5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID

56172-36-2

Step 1: Preparation of 5-hydroxybenzofuran-2-carboxylic acid. 5-Methoxybenzofuran-2-carboxylic acid (1.0 g, 5.2 mmol) was dissolved in anhydrous dichloromethane (25 ml) and the solution was cooled to -78°C. A 1 M solution of boron tribromide dichloromethane (15.6 ml) was added slowly and dropwise under nitrogen protection. The reaction mixture was gradually warmed to room temperature and stirred continuously at this temperature for 4 hours. Upon completion of the reaction, the reaction was quenched with aqueous ammonium chloride solution (20 ml) and subsequently extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous sodium sulfate. After treatment, 0.9 g (100% yield) of the crude product of 5-hydroxybenzofuran-2-carboxylic acid was obtained.1H NMR (CD3OD) δ = 6.84 (dd, 1H), 6.95 (d, 1H), 7.17 (s, 1H), 7.32 (d, 1H).

References[1] Patent: US2005/26969, 2005, A1. Location in patent: Page/Page column 12
[2] Patent: WO2008/157270, 2008, A1. Location in patent: Page/Page column 74-75
5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials5-METHOXYBENZOFURAN-2-CARBOXYLIC ACID, ETHYL ESTER-->5-Methoxybenzofuran-2-carboxylic acid-->Boron tribromide-->Dichloromethane
Tag:5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID(56172-36-2) Related Product Information
5-ETHOXY-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID ETHYL ESTER 5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID 5-METHOXYBENZOFURAN-2-CARBOXYLIC ACID, ETHYL ESTER 5-METHOXY-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID 5-Methoxybenzofuran-2-carboxylic acid 5-METHOXY-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID ETHYL ESTER 5-ETHOXY-3-METHYL-BENZOFURAN-2-CARBOXYLIC ACID