Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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
Mol File:
56172-36-2.mol
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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
pka
3.06±0.30(Predicted)
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5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID Usage And Synthesis

Synthesis

10242-08-7

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

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