Sodium Hydroxide → 4-(3-chloro-4-fluorophenyl)-1H-indole

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

To a mixture of 4-(4,4,5,5-tetramethyl-[1,3,2) dioxaborolan-2-yl) 1H-indole (3, 3.00 g, 12.34 mmol), and 4-bromo-2-chloro-fluorobenzene (2.58 g, 12.34 mmol) in THF (42 mL)) were added Palladium catalyst Pd(PPh3)4 (0.428 g, 0.37 mmol) and the freshly prepared sodium hydroxide solution (1.50 g, 37.02 mmol in 17 mL water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 75° C. oil bath for 15 hours. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed by brine, dried over Na2SO4, and concentrated. The crude product was purified by a silica gel column eluting with hexanes—EtOAc (9:1) to provide 2.11 g (70%) of the product 43-chloro-4-fluoro-phenyl)-1H-indole as a white solid.

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