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4-BROMO-2-METHOXYBENZYL ALCOHOL 97

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4-BROMO-2-METHOXYBENZYL ALCOHOL 97 Basic information

Product Name:
4-BROMO-2-METHOXYBENZYL ALCOHOL 97
Synonyms:
  • 4-BROMO-2-METHOXYBENZYL ALCOHOL 97
  • (4-broMo-2-Methoxyphenyl)Methanol
  • 4-Bromo-2-methoxybenzyl alcohol 97%
  • (4-Bromo-2-methoxyphenyl)
  • 4-Bromo-2-methoxybenzyl alcohol≥ 99% (GC)
  • Benzenemethanol, 4-bromo-2-methoxy-
  • 4-Bromo-2-methoxybenzyl alcohol
CAS:
17102-63-5
MF:
C8H9BrO2
MW:
217.06
Product Categories:
  • Alcohols
  • C7 to C8
  • Oxygen Compounds
  • Building Blocks
  • C7 to C8
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
17102-63-5.mol
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4-BROMO-2-METHOXYBENZYL ALCOHOL 97 Chemical Properties

Melting point:
66-70 °C (lit.)
Boiling point:
291℃
Density 
1.513
Flash point:
130℃
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
14.04±0.10(Predicted)
Appearance
White to off-white Solid
Water Solubility 
Insoluble in water.
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
24/25
WGK Germany 
2
HS Code 
29094990
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4-BROMO-2-METHOXYBENZYL ALCOHOL 97 Usage And Synthesis

Chemical Properties

Colorless to light yellow fine crystalline powder

Uses

It is used in azaquinone-methide-mediated depolymerization of aromatic carbamate oligomers.

Synthesis

139102-34-4

17102-63-5

General procedure for the synthesis of 4-bromo-2-methoxybenzenemethanol from methyl 4-bromo-2-methoxybenzoate: To a solution of methyl 4-bromo-2-methoxybenzoate (7.14 g, 29 mmol) in tetrahydrofuran (THF, 35 mL) was slowly added a THF solution of 2 M lithium borohydride (LiBH4) (35 mL, 70 mmol, 2.4 equiv). The reaction mixture was heated to reflux at 60 °C for 16 hours. Upon completion of the reaction, the mixture was cooled to room temperature and the solvent was evaporated under reduced pressure. The residue was dissolved in 5% aqueous acetic acid (pH adjusted to 6) and stirred for 15 minutes. Subsequently, the aqueous layer was extracted with ethyl acetate (EtOAc, 2 x 50 mL), the organic phases were combined and washed with saturated brine, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated to give the crude product as a tan oil. The crude product was purified by fast column chromatography using 5% ethyl acetate in hexane solution as eluent to give 5.96 g (94% yield) of the target product 4-bromo-2-methoxybenzenemethanol as a white solid: Thin Layer Chromatography (TLC) Rf value 0.30 (10% ethyl acetate/hexane); 1H NMR (CDCl3) δ 7.30 (d, 1H), 7.14 (d, 1H), 7.11 (d, 1H). 1H), 7.11 (s, 1H), 5.09 (t, 1H), 4.42 (d, 2H), 3.77 (s, 3H).

References

[1] Bioorganic and Medicinal Chemistry, 2014, vol. 22, # 1, p. 419 - 434
[2] Journal of Medicinal Chemistry, 1992, vol. 35, # 4, p. 734 - 740
[3] Patent: WO2006/60461, 2006, A1. Location in patent: Page/Page column 197
[4] ChemMedChem, 2010, vol. 5, # 1, p. 65 - 78
[5] Patent: WO2012/66335, 2012, A1. Location in patent: Page/Page column 54

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