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ChemicalBook CAS DataBase List 5-Bromo-3-cyano-2-hydroxypyridine
405224-22-8

5-Bromo-3-cyano-2-hydroxypyridine synthesis

2synthesis methods
20577-27-9 Synthesis
2-Hydroxy-3-cyanopyridine

20577-27-9
167 suppliers
$14.00/1g

5-Bromo-3-cyano-2-hydroxypyridine

405224-22-8
106 suppliers
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Yield:405224-22-8 88%

Reaction Conditions:

Stage #1: pyrid-2-one-3-carbonitrilewith acetic acid at 130;
Stage #2: with bromine for 3 h;

Steps:

1.2 Step 2: 5-bromo-2-oxo-1,2-dihydropyridine-3-carbonitrile

Acetic acid (34 ml) was added to 2-oxo-1,2-dihydropyridine-3-carbonitrile (6.28 g, 0.052 mol) and the mixture was heated to 130°C. When the solid was dissolved, bromine (12.5 g, 0.078 mol) was added slowly and stirred at the same temperature for 3 hours.After the reaction solution was cooled to room temperature, dichloromethane and water were added. The organic layer was separated and the aqueous layer was washed with dichloromethane. The organic layer was collected, washed with brine, dried over anhydrous sodium sulfate and concentrated to give the desired compound (9.11 g, 88% yield) as a yellow solid.

References:

KR101936851,2019,B1 Location in patent:Paragraph 0173; 0181-0184

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