ChemicalBook--->CAS DataBase List--->159870-80-1

159870-80-1

159870-80-1 Structure

159870-80-1 Structure
IdentificationBack Directory
[Name]

5-FLUORO-2-IODOPYRIDINE
[CAS]

159870-80-1
[Synonyms]

5-FLUORO-2-IODOPYRIDINE
2-Iodo-5-Fluoropyridine
Pyridine, 5-fluoro-2-iodo-
5-Fluoro-2-iodopyridine 97%
5-FLUORO-2-IODOPYRIDINE ISO 9001:2015 REACH
[Molecular Formula]

C5H3FIN
[MDL Number]

MFCD07787574
[MOL File]

159870-80-1.mol
[Molecular Weight]

222.99
Chemical PropertiesBack Directory
[Boiling point ]

197℃
[density ]

2.046
[Fp ]

73℃
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

-0.58±0.10(Predicted)
[color ]

yellow to off-white solid
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

5-Fluoro-2-iodopyridine(159870-80-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Bromo-5-fluoropyridine

41404-58-4

5-Fluoro-2-iodopyridine

159870-80-1

General procedure for the synthesis of 5-fluoro-2-iodopyridine from 2-bromo-5-fluoropyridine: under nitrogen protection, Cu2O (7.2 mg, 10 mol%), L-proline (11.5 mg, 20 mol%), 2-bromo-5-fluoropyridine (0.50 mmol), potassium iodide (KI, 249 mg, 0.75 mmol) and ethanol (EtOH, 1.5 mL). After sealing the Schlenk tube with a PTFE valve, the reaction mixture was stirred at 110 °C. The reaction process was monitored by gas chromatography (GC) analysis. Upon completion of the reaction, the yield was determined by GC using an appropriate internal standard (e.g., chlorobenzene or 1-chloro-4-methylbenzene) for highly volatile products; or the solvent was removed by distillation under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent ratio of petroleum ether/ethyl acetate = 10/1) to give the target product 5-fluoro-2-iodopyridine.

[References]

[1] Catalysis Today, 2016, vol. 274, p. 129 - 132
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