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1214385-51-9

1214385-51-9 Structure

1214385-51-9 Structure
IdentificationBack Directory
[Name]

5-BroMo-6-hydroxypicolinic acid
[CAS]

1214385-51-9
[Synonyms]

5-BroMo-6-hydroxypicolinic acid
5-bromo-6-hydroxypyridine-2-carboxylic acid
5-bromo-6-oxo-1,6-dihydropyridine-2-carboxylic acid
2-Pyridinecarboxylic acid, 5-bromo-1,6-dihydro-6-oxo-
[Molecular Formula]

C6H4BrNO3
[MDL Number]

MFCD13185807
[MOL File]

1214385-51-9.mol
[Molecular Weight]

218
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

5-BroMo-6-hydroxypicolinic acid(1214385-51-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Hydroxypicolinic acid

19621-92-2

5-BroMo-6-hydroxypicolinic acid

1214385-51-9

General procedure for the synthesis of 5-bromo-6-hydroxypyridinecarboxylic acid from 6-hydroxypyridine-2-carboxylic acid: bromine (115 g, 720 mmol) was added dropwise to a suspension of 6-oxo-1,6-dihydropyridine-2-carboxylic acid (25 g, 180 mmol) in acetic acid (400 mL). The reaction mixture was heated to 80 °C and kept for 16 hours. Upon completion of the reaction, the mixture was concentrated to dryness under reduced pressure. The residue was ground with tert-butyl methyl ether (200 mL) and subsequently filtered. The filter cake was washed with tert-butyl methyl ether (3 x 100 mL) to give a gray solid product. Yield: 39.0 g, 179 mmol, 99% yield. The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.03 (d, J = 7.3 Hz, 1H), 6.83 (d, J = 7.3 Hz, 1H).

[References]

[1] Patent: US2016/222007, 2016, A1. Location in patent: Paragraph 0354; 0355
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