ChemicalBook--->CAS DataBase List--->59717-96-3

59717-96-3

59717-96-3 Structure

59717-96-3 Structure
IdentificationBack Directory
[Name]

5-bromo-2-phenoxypyridine
[CAS]

59717-96-3
[Synonyms]

5-bromo-2-phenoxypyridine
Pyridine,5-bromo-2-phenoxy-
[Molecular Formula]

C11H8BrNO
[MDL Number]

MFCD12761236
[MOL File]

59717-96-3.mol
[Molecular Weight]

250.09
Chemical PropertiesBack Directory
[Boiling point ]

310.0±22.0 °C(Predicted)
[density ]

1.476±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

0.18±0.22(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Hazard InformationBack Directory
[Synthesis]

2,5-Dibromopyridine

624-28-2

Phenol

108-95-2

5-bromo-2-phenoxypyridine

59717-96-3

2,5-dibromopyridine (237 mg, 1 mmol, 1.0 equiv) and phenol (140 mg, 1.5 mmol, 1.5 equiv) were added with copper powder (32.5 mg, 0.5 mmol, 0.5 equiv), cuprous iodide (95 mg, 0.5 mmol, 0.5 equiv) and cesium carbonate (978 mg. 3.0 mmol, 3.0 equiv) in N-methylpyrrolidone (NMP, 10 mL). The reaction mixture was heated to 135 °C under nitrogen protection and maintained at this temperature for 5 h of reaction. After completion of the reaction, the solid insoluble material was removed by filtration and the filtrate was concentrated. Purification by column chromatography (eluent: ethyl acetate/petroleum ether = 10/1, v/v) afforded 5-bromo-2-phenoxypyridine as a brown solid (200 mg, 84.4% yield).

[References]

[1] Tetrahedron, 2013, vol. 69, # 1, p. 327 - 333
[2] Patent: CN108069974, 2018, A. Location in patent: Paragraph 0162-0165
[3] Patent: WO2018/35061, 2018, A1. Location in patent: Paragraph 0358
[4] Journal of Organometallic Chemistry, 2003, vol. 677, # 1-2, p. 57 - 72
[5] Patent: CN106146518, 2016, A. Location in patent: Paragraph 0038; 0039; 0040; 0041; 0042; 0043
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