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6-FLUORO-4-HYDROXYCOUMARIN

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6-FLUORO-4-HYDROXYCOUMARIN Basic information

Product Name:
6-FLUORO-4-HYDROXYCOUMARIN
Synonyms:
  • JRH-01309, 6-Fluoro-4-hydroxy-2H-chromen-2-one, 97%
  • 6-Fluoro-4-hydroxy-2H-1-Benzopyran-2-one
  • 6-FLUORO-4-HYDROXY-2H-CHROMEN-2-ONE
  • 6-FLUORO-4-HYDROXYCOUMARIN
  • 2H-1-Benzopyran-2-one, 6-fluoro-4-hydroxy-
  • 6-Fluoro-4-hydroxycoumarine
  • 6- Fluoro- 4- hydroxy coumarain
  • 6-Fluro-4-hydroxycoumarin
CAS:
1994-13-4
MF:
C9H5FO3
MW:
180.13
Product Categories:
  • Building Blocks
  • Coumarins
  • Heterocyclic Building Blocks
  • API intermediates
Mol File:
1994-13-4.mol
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6-FLUORO-4-HYDROXYCOUMARIN Chemical Properties

Melting point:
248-251 °C(lit.)
Boiling point:
354.0±42.0 °C(Predicted)
Density 
1.549±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
4.50±1.00(Predicted)
color 
White to Light yellow
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Safety Information

Hazard Codes 
Xi
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
2932209090

MSDS

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6-FLUORO-4-HYDROXYCOUMARIN Usage And Synthesis

Synthesis

394-32-1

105-58-8

1994-13-4

5-Fluoro-2-hydroxyacetophenone (1.54 g, 10 mmol) and diethyl carbonate (2.42 mL, 20 mmol) were dissolved in anhydrous tetrahydrofuran (30 mL) in a dry flask. The above solution was added dropwise to a rapidly stirred solution of potassium tert-butanolate tetrahydrofuran (1.0 M, 30 mL) through a cannula. The reaction was stirred overnight (10 hours) at room temperature and under positive pressure protection with nitrogen. Upon completion of the reaction, the crude product was concentrated under reduced pressure and partitioned between methyl tert-butyl ether and water. The layers were separated and the organic phase was discarded. The aqueous phase was adjusted to pH 5 with hydrochloric acid and subsequently extracted three times with an equal volume of dichloromethane. The organic phases were combined, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford 6-fluoro-4-hydroxy-2H-benzopyran-2-one (1.4 g, 78% yield). Mass spectrum (ESI negative ion mode) m/e: 179.16 ([M-H]-).

References

[1] Journal of Medicinal Chemistry, 2009, vol. 52, # 22, p. 7142 - 7156
[2] Patent: WO2009/100250, 2009, A1. Location in patent: Page/Page column 57
[3] Organic and Biomolecular Chemistry, 2018, vol. 16, # 15, p. 2634 - 2638
[4] Patent: EP354693, 1990, A1
[5] Advanced Synthesis and Catalysis, 2013, vol. 355, # 13, p. 2550 - 2557

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