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1353776-73-4

Pyridine, 4-bromo-2-phenoxy- synthesis

3synthesis methods
58530-53-3 Synthesis
2,4-Dibromopyridine

58530-53-3
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$4.00/1g

Pyridine, 4-bromo-2-phenoxy-

1353776-73-4
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Yield:1353776-73-4 98%

Reaction Conditions:

with copper(l) iodide;N,N,N,N,-tetramethylethylenediamine;caesium carbonate in dimethyl sulfoxide at 110; for 24 h;Inert atmosphere;regioselective reaction;Reagent/catalyst;Solvent;

Steps:

4.1 General procedure for the copper-catalyzed coupling reaction of 2,x-dihalopyridines and phenols

General procedure: 2,4-Dibromopyridine (0.236 g, 1 mmol) and phenol (0.094 g, 1 mmol), CuI (19.0 mg, 0.1 mmol), TMEDA (11.6 mg, 0.1 mmol), and cesium carbonate (0.65 g, 2 mmol) were placed in DMSO (5 mL). The reaction was stirred at 110 °C under nitrogen atmosphere for 24 h. When the reaction mixture was cooled, the reaction mixture was filtered. The mixture was dissolved with dichloromethane (25 mL). Then the mixture was washed with brine (3×30 mL). The organic phase was dried over sodium sulfate. After evaporation of the solvent, the mixture was subjected to column chromatography with petroleum ether/ethyl acetate (20:1) as eluent to give pure product

References:

Zhou, Qizhong;Zhang, Bin;Du, Tieqi;Gu, Haining;Ye, Yuyuan;Jiang, Huajiang;Chen, Rener [Tetrahedron,2013,vol. 69,# 1,p. 327 - 333]

58530-53-3 Synthesis
2,4-Dibromopyridine

58530-53-3
313 suppliers
$4.00/1g

Pyridine, 4-bromo-2-phenoxy-

1353776-73-4
1 suppliers
inquiry

1352327-92-4 Synthesis
2-Bromo-4-phenoxypyridine

1352327-92-4
4 suppliers
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