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3-bromo-6-ethoxy-2-Pyridinecarbonitrile synthesis

2synthesis methods
5-bromo-2-ethoxypyridine 1-oxide

55849-31-5
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7677-24-9 Synthesis
Trimethylsilyl cyanide

7677-24-9
367 suppliers
$19.00/5g

3-bromo-6-ethoxy-2-Pyridinecarbonitrile

1353777-41-9
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Yield:-

Reaction Conditions:

with triethylamine in acetonitrile at 100; for 24 h;

Steps:

XXXVII.1.b

b)1.00 g (4.59 mmol) 5-bromo-2-ethoxy-pyridine-1-oxide, 2.46 mL (18.3 mmol) trimethylsilyl cyanide and 1.92 mL (13.8 mmol) TEA in 10 mL ACN are stirred together at 100° C. for 24 h. Then the volatile components are removed in vacuo and the residue is dissolved in DCM, washed with aq. NaHCO3 solution, dried with MgSO4 and filtered through a plug of silica gel. Then the solvent is removed in vacuo.C8H7BrN2O (M=227.1 g/mol), ESI-MS: 227 [M+H]+Rf (TLC): 0.85 (silica gel, PE /EtOAc 7 /3)

References:

US2012/157425,2012,A1 Location in patent:Page/Page column 66