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ethyl 2-(6-bromo-2-nitropyridin-3-yloxy)acetate synthesis

2synthesis methods
443956-08-9 Synthesis
6-Bromo-2-nitro-pyridin-3-ol

443956-08-9
149 suppliers
$11.00/250mg

105-36-2 Synthesis
Ethyl bromoacetate

105-36-2
343 suppliers
$5.00/5G

ethyl 2-(6-bromo-2-nitropyridin-3-yloxy)acetate

443956-09-0
12 suppliers
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Yield:443956-09-0 89%

Reaction Conditions:

with potassium carbonate in acetone; for 10 h;Heating / reflux;

Steps:

3.b

2-Bromo-5-hydroxy-6-nitropyridine (30 g, 0.14 mole) was suspended in acetone(200 ml), and potassium carbonate (39 g, 0.28 mole) was added, followed by ethyl bromoacetate (15.7 ml, 0.14 mmole). The reaction was heated at reflux for 10 hr, then was cooled to room temperature and diluted with Et2θ. The precipitate was removed by suction filtration, and the filtrate was concentrated in vacuo to afford material (38 g, 89%), which was used without further purification: MS (ES) m/z 305.0 (M + H)+.

References:

WO2006/81178,2006,A2 Location in patent:Page/Page column 22