| Identification | Back 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 Properties | Back 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 |
| Hazard Information | Back Directory | [Synthesis]
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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