ChemicalBook--->CAS DataBase List--->22282-65-1

22282-65-1

22282-65-1 Structure

22282-65-1 Structure
IdentificationBack Directory
[Name]

4-Iodo-2-methylpyridine
[CAS]

22282-65-1
[Synonyms]

4-Iodo-2-methylpyridine
Pyridine, 4-iodo-2-methyl-
4-Iodo-2-methylpyridine ISO 9001:2015 REACH
[Molecular Formula]

C6H6IN
[MDL Number]

MFCD09702484
[MOL File]

22282-65-1.mol
[Molecular Weight]

219.02
Chemical PropertiesBack Directory
[storage temp. ]

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

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

4-Iodo-2-methylpyridine(22282-65-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Chloro-2-picoline

3678-63-5

4-Iodo-2-methylpyridine

22282-65-1

General procedure for the synthesis of 2-methyl-4-iodopyridine from 4-chloro-2-methylpyridine: 4-chloro-2-methylpyridine (10 g, 78 mmol), sodium iodide (17.8 g, 118 mmol), and hydriodic acid (57%, 26 mL, 196 mmol) were heated and reacted in a sealed tube for 7 days at 140 °C. Upon completion of the reaction, the reaction mixture was slowly poured into ice water and neutralized with sodium hydroxide solution. Subsequently, the mixture was extracted three times with dichloromethane (300 mL each time). The organic phases were combined, dried with magnesium sulfate, filtered and concentrated under reduced pressure. The resulting product was an off-white solid (14.7 g, 85% yield) and could be used in subsequent reactions without further purification.

[References]

[1] Patent: WO2004/80998, 2004, A1. Location in patent: Page 27
[2] Patent: US2002/40040, 2002, A1
[3] Chemical & Pharmaceutical Bulletin, 1982, vol. 30, # 5, p. 1731 - 1737
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