4-BROMO-3-HYDROXYPYRIDINE
4-BROMO-3-HYDROXYPYRIDINE Basic information
- Product Name:
- 4-BROMO-3-HYDROXYPYRIDINE
- Synonyms:
-
- 4-BROMO-3-HYDROXYPYRIDINE
- 4-BROMO-3-PYRIDINOL
- 4-BROMO-3-HYDROXYOPYRIDINE
- 3-Pyridinol, 4-bromo-
- 4-Bromopyridin-3-ol
- 4-boro-3-hydroxypyridine
- 4-BROMO-3-HYDROXYPYRIDINE ISO 9001:2015 REACH
- CAS:
- 161417-28-3
- MF:
- C5H4BrNO
- MW:
- 174
- EINECS:
- 806-483-1
- Product Categories:
-
- Pyridines
- Pyridines, Pyrimidines, Purines and Pteredines
- pharmacetical
- Pyridine
- Chemical Amines
- Amines
- Aromatics
- Heterocycles
- Mol File:
- 161417-28-3.mol
4-BROMO-3-HYDROXYPYRIDINE Chemical Properties
- Melting point:
- 134-136°C
- Boiling point:
- 316.2±22.0 °C(Predicted)
- Density
- 1.788±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,2-8°C
- solubility
- Chloroform (Sparingly), Ethyl Acetate
- form
- Solid
- pka
- 6.57±0.10(Predicted)
- color
- White to Off-White
4-BROMO-3-HYDROXYPYRIDINE Usage And Synthesis
Chemical Properties
White Solid
Synthesis
98976-81-9
161417-28-3
The general procedure for the synthesis of 4-bromo-3-hydroxypyridine from the compound (CAS: 98976-81-9) is as follows: to a solution of 4-bromo-3-pyridinyl diethylcarbamate (1.24 g, 4.50 mmol) in methanol (10 mL) was added methanolic solution of sodium methanolate (2.04 g, 9.40 mmol) at 20°C and the resulting mixture was refluxed for 1.5 hours. Upon completion of the reaction, methanol was removed by distillation under reduced pressure, ethyl acetate (15 mL) and water (1 mL) were added, and then the pH was adjusted to 9 with 20% aqueous sulfuric acid. the organic layer was separated, and the residue was washed with ethyl acetate (3 x 5 mL). The organic layers were combined, dried and concentrated with anhydrous sodium sulfate. The crude product was purified by rapid chromatography on silica gel, eluting sequentially with hexane/ethyl acetate (1:1 and 1:2) to give 691 mg (89% yield) of 4-bromo-3-hydroxypyridine.TLC Rf value was 0.38 (1:2 hexane/ethyl acetate). Mass spectra (DCI/NH3) m/e 174 (with 79 Br) and 176 (M+H)+ (with 81 Br).1H NMR (CDCl3, 300 MHz) δ: 8.43 (d, J=1.5 Hz, 1H, ArH), 8.02 (d, J=7.2 Hz, 1H, ArH), 7.54 (dd, J=7.2,1.5 Hz. 1H, ArH).
References
[1] Patent: US5914328, 1999, A
[2] Patent: US5948793, 1999, A
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