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3-HYDROXY-2-PHENYLPYRIDINE

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3-HYDROXY-2-PHENYLPYRIDINE Basic information

Product Name:
3-HYDROXY-2-PHENYLPYRIDINE
Synonyms:
  • 2-phenyl-3-pyridino
  • 2-Phenyl-3-hydroxypyridine
  • 3-Pyridinol, 2-phenyl-
  • 4-N-(2-bromophenyl)pyrido[4,3-d]pyrimidine-4,7-diamine
  • 3-HYDROXY-2-PHENYLPYRIDINE
  • 2-PHENYL-3-PYRIDINOL
  • 2-PHENYL-PYRIDIN-3-OL
  • 3-HYDROXY-2-PHENYLPYRIDINE ISO 9001:2015 REACH
CAS:
3308-02-9
MF:
C11H9NO
MW:
171.2
Product Categories:
  • Pyridines, Pyrimidines, Purines and Pteredines
  • pharmacetical
Mol File:
3308-02-9.mol
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3-HYDROXY-2-PHENYLPYRIDINE Chemical Properties

Melting point:
205 °C
Boiling point:
320 °C
Density 
1.169±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
8.23±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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3-HYDROXY-2-PHENYLPYRIDINE Usage And Synthesis

Synthesis Reference(s)

Tetrahedron, 48, p. 8117, 1992 DOI: 10.1016/S0040-4020(01)80481-6

Synthesis

40263-57-8

98-80-6

3308-02-9

To a stirred solution of 2-iodo-3-hydroxypyridine (5.0 g, 22.624 mmol) in benzene (50 ml) was added phenylboronic acid (3.03 g, 24.85 mmol) and 2M Na2CO3 solution (20 mL) sequentially at 25 °C. The reaction system was protected and degassed with argon for 15 min. Tetrakis(triphenylphosphine)palladium (Pd(PPh3)4, 1.3 g, 5 mol%) was then added and degassing continued for 10 minutes. The reaction mixture was heated to reflux for 4 hours. After completion of the reaction, it was cooled to room temperature, water was added and extracted with ethyl acetate (EtOAc). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by solvent milling with methyl tert-butyl ether (MTBE)/dichloromethane (DCM) mixture to give 3-hydroxy-2-phenylpyridine (3.2 g).LCMS detection showed a molecular ion peak of 172 (M + H).

References

[1] Patent: WO2014/186035, 2014, A1. Location in patent: Page/Page column 175; 178; 179

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