Catalytic C-C Coupling Reactions at Nickel by C-F Activation of a Pyrimidine in the Presence of a C-Cl Bond: The Crucial Role of Highly Reactive Fluoro Complexes
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Treatment of [Ni(COD)2] (COD = 1,5-cyclooctadiene) with 5-chloro-2,4,6-trifluoropyrimidine(1) in the presence of PiPr3 or PPh3 effects the formation of the fluoro complexes trans-[NiF(4-C4N2ClF2)(PiPr3)2] (3) and trans-[NiF(4-C4N2ClF2)(PPh3)2] (4). The chloro complextrans-[NiCl(4-C4N2ClF2)(PPh3)2] (5) can be prepared by reaction of 4 with Me3SiCl. Incontrast, a reaction of 1 with [Pd(PPh3)4] leads to the insertion of a {Pd(PPh3)2} unit intothe C-Cl bond yielding trans-[PdCl(5-C4N2F3)(PPh3)2] (6). Treatment of 4 with an excess ofTolB(OH)2 at 273 K results in the slow formation of trans-[NiF(4-C4N2TolClF)(PPh3)2] (7)and subsequently 5-chloro-2-fluoro-4,6-ditolylpyrimidine (8). Quenching of a solution of 7with Me3SiCl leads to the chloro derivative trans-[NiCl(4-C4N2TolClF)(PPh3)2] (9). Treatmentof 4 with PhB(OH)2 followed by addition of Me3SiCl gives the complex trans-[NiCl(4-C4N2PhClF)(PPh3)2] (10). In catalytic experiments, 1 is converted with the boronic acidsTolB(OH)2, PhB(OH)2, and p-F3CC6H4B(OH)2 into the 5-chloro-2-fluoro-4,6-diarylpyrimidines8, 11, and 12 in 73%, 88%, and 37% yield, respectively, when 10% of 4 is employed as catalyst.The molecular structures of the complexes 5, 6, and 10 have been determined by X-raycrystallography. The studies reported in this paper represent the first catalytic C-C couplingreactions involving the activation of a C-F bond in the presence of a thermodynamicallyweaker C-Cl bond. They provide a route to access 5-chloro-2-fluoro-4,6-diarylpyrimidines,which have not been described before. There is considerable evidence that the presence ofthe fluoro ligand in 4 is crucial for the transmetalation step to occur and for the catalyticcycle to proceed.

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