Reaktion #1131177

Reaktionsgleichung

6-chloro-pyridin-3-ylamine

I2

→

6-chloro-2-iodo-pyridin-3-ylamine

Ausbeute 86.4%

Lösungsmittel

EtOH

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe solvent was removed by evaporation under vacuum
2. 2
   workup.ADDITIONWater (100 mL) and EtOAc (200 mL) were added to the residue
3. 3
   SonstigeThe organic layer was separated
4. 4
   Extraktionthe aqueous layer was extracted with EtOAc (100 mL×3)
5. 5
   TrocknenThe combined organic layers were dried over anhydrous Na2SO4
6. 6
   Sonstigeevaporated under vacuum
7. 7
   Sonstigeto give the crude product, which
8. 8
   Sonstigewas purified by column chromatography on silica gel (Petroleum ether/Ethyl acetate 7:1)

Vorschrift

To a solution of 6-chloro-pyridin-3-ylamine (10.0 g, 77.8 mmol) in EtOH (150 mL) was added Ag2SO4 (12.1 g, 38.9 mmol) and I2 (23.7 g, 93.4 mmol) at room temperature. The mixture was stirred at 20° C. overnight. The solvent was removed by evaporation under vacuum. Water (100 mL) and EtOAc (200 mL) were added to the residue. The organic layer was separated and the aqueous layer was extracted with EtOAc (100 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and evaporated under vacuum to give the crude product, which was purified by column chromatography on silica gel (Petroleum ether/Ethyl acetate 7:1) to give 6-chloro-2-iodo-pyridin-3-ylamine (17.1 g, 86%). 1H NMR (DMSO, 300 MHz) δ 7.16 (d, J=8.4 Hz, 1H), 7.01 (d, J=8.4 Hz, 1H), 5.57 (s, 2H).

Quelle