Basic information Safety Supplier Related

1,2-Benzisoxazol-6-ol

Basic information Safety Supplier Related

1,2-Benzisoxazol-6-ol Basic information

Product Name:
1,2-Benzisoxazol-6-ol
Synonyms:
  • 6-Hydroxy-1,2-benzisoxazole
  • 1,2-benzisoxazol-6-ol(SALTDATA: FREE)
  • benzo[d]isoxazol-6-ol
  • 1,2-Benzisoxazol-6-ol
  • 2,6-dihydro-1,2-benzoxazol-6-one
CAS:
65685-55-4
MF:
C7H5NO2
MW:
135.12
Mol File:
65685-55-4.mol
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1,2-Benzisoxazol-6-ol Chemical Properties

Boiling point:
300 ºC
Density 
1.378
Flash point:
135 ºC
storage temp. 
2-8°C
form 
solid
color 
White
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HazardClass 
IRRITANT
HS Code 
2934999090
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1,2-Benzisoxazol-6-ol Usage And Synthesis

Synthesis

5399-68-8

65685-55-4

General procedure for the synthesis of 1,2-benzisoxazol-6-ol from 2,4-dihydroxybenzaldehyde oxime: 2,4-dihydroxybenzaldehyde oxime (2.0 mmol) was dissolved in 5 mL of anhydrous dichloromethane (DCM), and the solution was placed in a round bottom flask that had been pre-oven dried. A DCM solution of trifluoromethanesulfonic anhydride (2.0 mmol) was slowly added to the reaction mixture under nitrogen protection and the titration process was continued for 15 min. The reaction mixture was stirred at room temperature and the reaction process was monitored by thin layer chromatography (TLC) and gas chromatography-mass spectrometry (GC-MS) (see Table 1). Upon completion of the reaction, the reaction mixture was poured into crushed ice (100 mL), neutralized with 10% sodium bicarbonate (NaHCO3) solution (20 mL), and subsequently extracted with dichloromethane (3 × 15 mL). The organic phases were combined and purified by column chromatography using hexane-ethyl acetate (80:20, v/v) as eluent to afford the target product 1,2-benzisoxazol-6-ol. All the synthesized 1,2-benzisoxazole derivatives were characterized by GC-MS, nuclear magnetic resonance hydrogen spectroscopy (1H NMR) and carbon spectroscopy (13C NMR) as well as by elemental analysis, and the obtained data were validated by comparing them with real samples.

References

[1] Synthetic Communications, 2014, vol. 44, # 4, p. 547 - 555
[2] Tetrahedron Letters, 2006, vol. 47, # 47, p. 8247 - 8250
[3] Australian Journal of Chemistry, 1977, vol. 30, p. 1847 - 1850

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