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ChemicalBook CAS DataBase List 5-Bromonicotinic acid

5-Bromonicotinic acid synthesis

9synthesis methods
28733-43-9 Synthesis
5-Bromonicotinamide

28733-43-9
202 suppliers
$7.00/1g

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Yield:20826-04-4 98%

Reaction Conditions:

with acetic acid;isopentyl nitrite at 80; for 24 h;Inert atmosphere;

Steps:

5-Bromo-3-pyridinecarboxylic acid (12)

5-Bromo-3-pyridinecarboxamide (0.2010 g, 1 mmol) wasdissolved in acetic acid (2 mL), and to the stirring solution was added amyl nitrite (0.40 mL, 3 mmol).The reaction was placed under N2 atmosphere and heated to 80 °C for 24 hours, whereupon thereaction was complete by consumption of starting material by TLC. The solution was condensed andco-evaporated with toluene (2 x 5 mL), then purified via trituration from EtOAc and Hexane. Theresulting suspension was filtered to afford off-white powder (0.1993 g, 0.98 mmol). 1H-NMR (400MHz; MeOD): δ 9.12 (d, J = 1.7 Hz, 1H), 8.93 (d, J = 2.3 Hz, 1H), 8.62 (dd, J = 2.3, 1.7 Hz, 1H); MSm/z 200 (M-, 100%); melting point: 180-183 °C; IR (neat) νmax 3033 (w br, O-H stretch), 1673 (s,C=O stretch), 1287 (acyl C-O), 688 (s, aromatic C-H) cm-1

References:

Potter, Garrett T.;Jayson, Gordon C.;Miller, Gavin J.;Gardiner, John M. [Tetrahedron Letters,2015,vol. 56,# 37,p. 5153 - 5156] Location in patent:supporting information

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