4-BROMO-2-METHOXYBENZYL ALCOHOL 97
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
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.
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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