| Identification | Back Directory | [Name]
5-BROMO-3-CHLORO-2-METHYLPYRIDINE | [CAS]
914358-72-8 | [Synonyms]
5-BroMo-3-chloro-2-Methyl...
2-Methyl-3-chloro-5-bromopyridine
5-BROMO-3-CHLORO-2-METHYLPYRIDINE
Pyridine, 5-bromo-3-chloro-2-methyl-
5-BROMO-3-CHLORO-2-METHYLPYRIDINE ISO 9001：2015 REACH | [Molecular Formula]
C6H5BrClN | [MDL Number]
MFCD09031417 | [MOL File]
914358-72-8.mol | [Molecular Weight]
206.47 |
| Chemical Properties | Back Directory | [Boiling point ]
208℃ | [density ]
1.624 | [Fp ]
80℃ | [storage temp. ]
Inert atmosphere,Room Temperature | [pka]
1.31±0.20(Predicted) | [Appearance]
White to off-white Solid |
| Hazard Information | Back Directory | [Uses]
5-BROMO-3-CHLORO-2-METHYLPYRIDINE is a heterocyclic compound that
belongs to the pyridine family. It is characterized by its unique
structure and functional groups, including a bromo and chloro
substituent, which make it highly reactive and versatile.
It serves as an important intermediate in
the synthesis of pharmaceuticals, agrochemicals, and specialty
chemicals, and is also used as a reagent in organic synthesis and
medicinal chemistry. | [Synthesis]
General procedure for the synthesis of 2-methyl-3-chloro-5-bromopyridine from diethyl 2-(5-bromo-3-chloropyridin-2-yl)malonate: firstly, impure diethyl 2-(5-bromo-3-chloropyridin-2-yl)malonate (Intermediate 42, 0.41 g, 1.2 mmol) was dissolved in a concentrated aqueous hydrochloric acid solution (3 mL), and heated and refluxed for 3 hours. Upon completion of the reaction, volatiles were removed by vacuum distillation and the residue was co-evaporated with acetonitrile. Subsequently, the resulting monodeoxycarboxylic acid solid was dissolved in dioxane (4.5 mL) and heated to reflux overnight. The volatiles were again removed by vacuum distillation. Finally, the residue was purified by fast chromatography (using 4 g SiO2, heptane/EtOAc gradient elution) to afford the target product 2-methyl-3-chloro-5-bromopyridine (0.12 g, 51% yield). The product was characterized by 1H NMR (500 MHz, CDCl3): δ 2.60 (s, 3H), 7.82 (d, 1H), 8.46 (d, 1H); the mass spectrum (CI) showed m/z 206 [M + H]+. | [References]
[1] Patent: US2012/165347, 2012, A1. Location in patent: Page/Page column 32 |
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