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717843-51-1

717843-51-1 Structure

717843-51-1 Structure
IdentificationBack Directory
[Name]

3-BROMO-2-METHOXY-4-PICOLINE
[CAS]

717843-51-1
[Synonyms]

3-BROMO-2-METHOXY-4-PICOLINE
Pyridine, 3-bromo-2-methoxy-4-methyl-
[Molecular Formula]

C7H8BrNO
[MDL Number]

MFCD08061305
[MOL File]

717843-51-1.mol
[Molecular Weight]

202.05
Chemical PropertiesBack Directory
[Boiling point ]

223.4±35.0 °C(Predicted)
[density ]

1.452±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

liquid
[pka]

1.70±0.18(Predicted)
[color ]

Colourless to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P301+P312
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

3-BROMO-2-METHOXY-4-PICOLINE(717843-51-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-BROMO-2-CHLORO-4-PICOLINE

55404-31-4

3-BROMO-2-METHOXY-4-PICOLINE

717843-51-1

(2) Synthesis of 3-bromo-2-methoxy-4-methylpyridine: In a dry reaction flask, 3-bromo-2-chloro-4-methylpyridine (1 g) was dissolved in N,N-dimethylformamide (DMF, 5.6 mL). Subsequently, sodium methanol (28% methanol solution, 4.6 mL) was slowly added to this solution. The reaction mixture was placed in an oil bath at 100°C and the reaction was stirred for 12 hours. After completion of the reaction, the mixture was cooled to room temperature and liquid-liquid partitioned with ethyl acetate and water. The organic layer was separated and dried with anhydrous magnesium sulfate. After filtration to remove the drier, the filtrate was concentrated under reduced pressure to give the crude product. The crude product was further purified by silica gel column chromatography with the eluent of ethyl acetate/n-heptane (gradient elution, 5% to 30%) to afford the target compound 3-bromo-2-methoxy-4-methylpyridine (1.1 g). The structure of the product was confirmed by 1H-NMR (400 MHz, CDCl3): δ (ppm) 2.40 (s, 3H, CH3), 4.00 (s, 3H, OCH3), 6.77 (d, J = 5.1 Hz, 1H, pyridine ring H), 7.94 (d, J = 5.1 Hz, 1H, pyridine ring H).

[References]

[1] Patent: US2013/143907, 2013, A1. Location in patent: Paragraph 0477; 0478
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