PYRIDINE, 2,6-DIFLUORO-4-IODO-

685517-67-3

685517-71-9

The general procedure for the synthesis of 2,6-difluoro-4-iodopyridine from 2,6-difluoro-3-iodopyridine was as follows: n-butyllithium (1.66 mL, 4.15 mmol, 2.5 mol/L hexane solution) was slowly added dropwise to a solution of tetrahydrofuran (THF, 2 mL) with diisopropylamine (1.30 mL, 4.15 mmol) at -78 °C. 25 minutes later, a solution of 2,6-difluoro-3-iodopyridine (1.00 g, 4.15 mmol) in THF (5 mL) was added dropwise to the above mixture via cannula. The reaction mixture was kept at -78 °C for 12 h. THF (2 mL) solution in water (0.2 mL, 11 mmol) was subsequently added and slowly warmed up to room temperature over a period of 1 h. The reaction was carried out at -78 °C for 1 h. The reaction was carried out in a controlled manner. Upon completion of the reaction, the reaction mixture was washed with 10% aqueous Na2SO3 solution (5 mL) and extracted with ethyl acetate (3 x 50 mL). The organic phases were combined and dried over anhydrous magnesium sulfate (MgSO4) and subsequently concentrated under reduced pressure. The target product 2,6-difluoro-4-iodopyridine was obtained by hexane crystallization as colorless crystals (740 mg, 74% yield). The product was characterized as follows: 1H NMR (400 MHz, CDCl3): δ 7.22 (t, 2H, J = 1.2 Hz); 13C NMR (100 MHz, CDCl3): δ 161.1 (dd, J = 250, 16 Hz, 2C), 115.6 (dd, J = 24, 10 Hz, 2C), 110.3; 19F NMR (376 MHz, CDCl3): δ -68.1; GC-MS m/z: Calculated value 241 [M+], measured value 241; Melting point: 78-80 °C.