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3-HYDROXY-4-IODOBENZYL ALCOHOL

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3-HYDROXY-4-IODOBENZYL ALCOHOL Basic information

Product Name:
3-HYDROXY-4-IODOBENZYL ALCOHOL
Synonyms:
  • 5-(HYDROXYMETHYL)-2-IODOPHENOL
  • 3-HYDROXY-4-IODOBENZYL ALCOHOL
  • RARECHEM AL BD 0964
  • Benzenemethanol,3-hydroxy-4-iodo-
  • 5-(Hydroxymethyl)-2-iodophenol 97%
  • 3-Hydroxy-4-iodobenzenemethanol
  • 3-Hydroxy-4-iodobenzyl alcohol, (3-Hydroxy-4-iodophenyl)methanol
  • 3-Hydroxy-4-iodobenz
CAS:
773869-57-1
MF:
C7H7IO2
MW:
250.03
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Methyl Halides
  • Phenyls & Phenyl-Het
  • Methyl Halides
  • Phenyls & Phenyl-Het
Mol File:
773869-57-1.mol
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3-HYDROXY-4-IODOBENZYL ALCOHOL Chemical Properties

Melting point:
148 °C
Boiling point:
273.9±25.0 °C(Predicted)
Density 
2.020±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.29±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

Hazard Note 
Harmful
HS Code 
2909500090
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3-HYDROXY-4-IODOBENZYL ALCOHOL Usage And Synthesis

Synthesis

58123-77-6

773869-57-1

The general procedure for the synthesis of 3-hydroxy-4-iodobenzyl alcohol from 3-hydroxy-4-iodobenzoic acid was as follows: to a solution of 3-hydroxy-4-iodobenzoic acid (20.9 g, 79.3 mmol) in anhydrous THF (160 mL) was slowly added a 1 M borane-THF solution (240 mL, 240 mmol). The reaction mixture was stirred at 60 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by careful addition of water and subsequently extracted twice with ethyl acetate. The organic phases were combined, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was removed by concentration under reduced pressure and the resulting residue was washed with diisopropyl ether and hexane to give 3-hydroxy-4-iodobenzenemethanol (17.4 g, 88% yield) as a white solid. The structure of the product was confirmed by 1H NMR (CDCl3): δ 1.69 (br, 1H), 4.64 (s, 2H), 5.33 (s, 1H), 6.70 (dd, J = 7.8, 1.5 Hz, 1H), 7.01 (d, J = 1.5 Hz, 1H), 7.63 (d, J = 7.8 Hz, 1H).

References

[1] Patent: EP2351743, 2011, A1. Location in patent: Page/Page column 117

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