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2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE

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2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE Basic information

Product Name:
2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE
Synonyms:
  • 2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE
  • Benzaldehyde, 2,6-difluoro-4-hydroxy- (9CI)
  • 3,5-Difluoro-4-formylphenol
  • 6-difluoro-4-hydroxybenzaldehyde
  • 2,6-Difluoro-4-hydroxybenzaldehyde ,97%
  • 2,6-difluoro-4-hydroxybenzaldehyde2,6-difluoro-4-hydroxybenzaldehyde
  • 2,6-Difluoro-4-hydroxybenzaldehyde 98%
  • Benzaldehyde, 2,6-difluoro-4-hydroxy-
CAS:
532967-21-8
MF:
C7H4F2O2
MW:
158.1
Product Categories:
  • ALDEHYDE
  • ALCOHOL
  • HALIDE
  • Aromatic Aldehydes & Derivatives (substituted)
Mol File:
532967-21-8.mol
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2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE Chemical Properties

Melting point:
179-182℃
Boiling point:
252.6±35.0 °C(Predicted)
Density 
1.464±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder
pka
5.80±0.23(Predicted)
color 
Off-white to cream
Sensitive 
Air Sensitive
CAS DataBase Reference
532967-21-8
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Safety Information

Hazard Codes 
Xi
Risk Statements 
20-36/37/38
Safety Statements 
22-36/37/39-45
Hazard Note 
Irritant
HS Code 
29124990
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2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE Usage And Synthesis

Chemical Properties

Brown to red powder

Synthesis

68-12-2

532967-21-8

General procedure for the synthesis of 2,6-difluoro-4-hydroxybenzaldehyde from N,N-dimethylformamide: At -78 °C, sec-butyllithium (1.3 M cyclohexane solution, 53 mL, 69.3 mmol) was slowly added to intermediates 19,1-(tert-butyldimethylsilyl)oxy-3,5-difluorobenzene (15.3 g, 62.6 mmol) and TMEDA (10.5 mL, 69.3 mmol) in a solution of tetrahydrofuran (200 mL) and stirred for 30 min at a maintained temperature of -78 °C. Subsequently, DMF (5.33 mL, 69.3 mmol) was added at the same temperature and stirring was continued for 1.5 hours. After the reaction was completed, 10% aqueous hydrochloric acid was added to adjust the pH to 4-5 (~200 mL) and then stirred at room temperature for 12 hours. The aqueous layer was extracted with ethyl acetate (200 mL) and the organic layer was separated. The organic layer was washed sequentially with saturated aqueous sodium bicarbonate, added sodium bicarbonate followed by water, and then adjusted the pH to 3-4 with hydrochloric acid, separated the organic layer, washed with brine, dried with anhydrous sodium sulfate, and finally evaporated in vacuum to obtain 2,6-difluoro-4-hydroxybenzaldehyde (9.7 g, 97% yield, 61.3 mmol) as a white solid.1H NMR (DMSO-d6) data: δ 11.54 (br.s, 1H, OH), 10.00 (s, 1H, CHO), 6.50-6.57 (m, 2H, Ar-H).

References

[1] Patent: WO2006/136924, 2006, A1. Location in patent: Page/Page column 136-137

2,6-DIFLUORO-4-HYDROXYBENZALDEHYDE Preparation Products And Raw materials

Raw materials

2,6-DIFLUORO-4-HYDROXYBENZALDEHYDESupplier

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