ChemicalBook--->CAS DataBase List--->1211516-25-4

1211516-25-4

1211516-25-4 Structure

1211516-25-4 Structure
IdentificationBack Directory
[Name]

2-broMo-3-Methyl-pyridine-3-carboxyl acid
[CAS]

1211516-25-4
[Synonyms]

6-BroMo-5-Methylpicolinic acid
2-broMo-3-Methyl-pyridine-3-carboxyl acid
6-BROMO-5-METHYL-PYRIDINE-2-CARBOXYLIC ACID
2-Pyridinecarboxylic acid, 6-bromo-5-methyl-
[Molecular Formula]

C7H6BrNO2
[MDL Number]

MFCD18257503
[MOL File]

1211516-25-4.mol
[Molecular Weight]

216.03
Chemical PropertiesBack Directory
[Boiling point ]

373.9±42.0 °C(Predicted)
[density ]

1.692±0.06 g/cm3(Predicted)
[storage temp. ]

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

3.42±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

2-Bromo-6-cyano-3-methylpyridine

450844-27-6

2-broMo-3-Methyl-pyridine-3-carboxyl acid

1211516-25-4

The general procedure for the synthesis of 6-bromo-5-methyl-pyridine-2-carboxylic acid from 5-methyl-6-bromo-pyridine-2-carbonitrile was as follows: 6-bromo-5-methyl-pyridine-2-carbonitrile (1.0 g, 5.0 mmol) was dissolved in an aqueous solution of sodium hydroxide (0.3 g, 7 mmol, 20 mL), and the reaction was stirred at 120 °C overnight. Upon completion of the reaction, the reaction mixture was adjusted to pH=3 with acid and subsequently extracted with ethyl acetate (3 x 15 mL). The organic phases were combined, washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to afford the target product 6-bromo-5-methyl-pyridine-2-carboxylic acid (0.7 g, 63.8% yield). Mass spectrometry (EI) analysis showed m/e 216.0 [M+H]+.

[References]

[1] Patent: US2012/316147, 2012, A1. Location in patent: Page/Page column 52
[2] Patent: WO2012/168350, 2012, A1. Location in patent: Page/Page column 114
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