Basic information Safety Supplier Related

3-HYDROXYBENZAMIDE

Basic information Safety Supplier Related

3-HYDROXYBENZAMIDE Basic information

Product Name:
3-HYDROXYBENZAMIDE
Synonyms:
  • 1-phenyl-5-(4-phenylphenyl)-3-pyrazolecarboxylic acid methyl ester
  • 3-HYDROXYBENZAMIDE
  • Benzamide, 3-hydroxy- (9CI)
  • BenzaMide, 3-hydroxy-
  • m-Hydroxybenzamide
  • 3- Hydroxy benzomide
  • Deferasirox 3-Hydroxy benzamide Impurity
CAS:
618-49-5
MF:
C7H7NO2
MW:
137.14
Product Categories:
  • AMIDE
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
Mol File:
618-49-5.mol
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3-HYDROXYBENZAMIDE Chemical Properties

Melting point:
170 °C
Boiling point:
318.3±25.0 °C(Predicted)
Density 
1.449 g/cm3
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
9.26±0.10(Predicted)
color 
White to Light yellow
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
26
HS Code 
2924.29.7790
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3-HYDROXYBENZAMIDE Usage And Synthesis

Synthesis

873-62-1

618-49-5

General procedure for the synthesis of 3-hydroxybenzamide from 3-hydroxybenzonitrile: 3-cyanophenol (295 mg, 2.48 mmol, 100 mol%) and sodium perborate tetrahydrate (NaBO3-4H2O, 1146 mg, 7.45 mmol, 300 mol%) were dissolved in water (8 mL) and heated to 50 °C. Methanol (14 mL) was then added slowly until the mixture became clear. The reaction mixture was stirred continuously at 50 °C for 70 hours. After completion of the reaction, excess methanol was removed by evaporation. The pH of the remaining mixture was adjusted with dilute hydrochloric acid (aq) to 5. Extraction was carried out with dichloromethane (12 mL) and ethyl acetate (5 x 15 mL). The organic phases were combined, washed with brine (25 mL) and dried over anhydrous sodium sulfate (Na2SO4). After filtration, the solvent was evaporated to give the target product, 3-hydroxybenzamide (49a), as a spectroscopically pure white solid (183 mg, 54% yield): melting point 165-168 °C; thin-layer chromatography Rf value (50% ethyl acetate/hexane) 0.10.

References

[1] RSC Advances, 2015, vol. 5, # 16, p. 12152 - 12160
[2] Tetrahedron, 1989, vol. 45, # 11, p. 3299 - 3306
[3] ChemMedChem, 2010, vol. 5, # 2, p. 213 - 231
[4] Patent: WO2008/129129, 2008, A1. Location in patent: Page/Page column 66

3-HYDROXYBENZAMIDESupplier

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