5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID
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
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)
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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5-HYDROXY-1-BENZOFURAN-2-CARBOXYLIC ACID(56172-36-2)Related Product Information
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