Basic information Safety Supplier Related

2,4-Difluoro-5-nitrophenol

Basic information Safety Supplier Related

2,4-Difluoro-5-nitrophenol Basic information

Product Name:
2,4-Difluoro-5-nitrophenol
Synonyms:
  • 2,4-Difluoro-5-nitrophenol
  • 2,4-Difluoro-5-hydroxynitrobenzene
  • Phenol, 2,4-difluoro-5-nitro-
  • ,4-Difluoro-5-nitrophenol
  • 2,4-Difluoro-5-nitrophenol,98%
CAS:
113512-57-5
MF:
C6H3F2NO3
MW:
175.09
Mol File:
113512-57-5.mol
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2,4-Difluoro-5-nitrophenol Chemical Properties

Melting point:
112-120℃
Boiling point:
160-162 °C(Press: 24 Torr)
Density 
1.619±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
6.81±0.24(Predicted)
Appearance
Light yellow to green yellow Solid
Water Solubility 
Sparingly soluble in water but readily soluble in organic solvents.
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Safety Information

HS Code 
2908990000
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2,4-Difluoro-5-nitrophenol Usage And Synthesis

Uses

2,4-Difluoro-5-nitrophenol may be used in chemical synthesis.

Synthesis

152169-43-2

113512-57-5

Using 2,4-difluorophenyl ethyl carbonate (3.1 g, 16 mmol) as raw material, nitric acid (0.78 ml, 19 mmol) was slowly added to a solution of sulfuric acid (10 mL) at 0 °C, keeping the reaction temperature at about 0 °C. After 15 min of reaction, the reaction was terminated by adding ice-cold water (70 mL), and the product was extracted with ethyl acetate (2 × 50 mL). The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and concentrated to give the nitro product as a thick syrup. The nitro product was dissolved in methanol (20 mL), solid sodium bicarbonate (4.0 g, 47 mmol) was added and stirred for 16 hours at room temperature. After completion of the reaction, the mixture was filtered and the filtrate was concentrated. The resulting solid was dissolved in water (20 ml) and acidified with 3M HCl solution to pH~5. The product was extracted with dichloromethane (3 x 25 mL), the organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and concentrated to give 2,4-difluoro-5-nitrophenol (2.34 g, 84% yield). The product was confirmed by 1H NMR (400 MHz, acetone-d6): δ 9.59 (s, 1H), 7.78 (t, J=7.2 Hz, 1H), 7.45 (t, J=10.4 Hz, 1H); mass spectrometry (ESI) m/z: 176.0 (M+H+).

References

[1] Patent: WO2013/36232, 2013, A2. Location in patent: Paragraph 00224
[2] Synthesis, 1997, # 12, p. 1446 - 1450
[3] Patent: EP755928, 1997, A1

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