Organometallic reagents are essential tools in synthetic chemistry. They work even better and more effectively in combination with alkali alkoxides. The exact nature of this effect has never been well understood. A team based in Switzerland has now performed a detailed study of the mechanism of reaction of aryl bromides with organo-magnesium reagents and lithium alkoxides. As reported in the journal Angewandte Chemie, a complex equilibrium of bimetallic intermediates plays a key role.
Substituted aromatic ring systems are an important class of building block for the synthesis of many products, including pharmaceuticals, agrochemicals, and natural substances. However, the required functional side groups cannot generally be hooked onto the ring systems in a simple way. A widely employed method uses a detour through a halogen/metal exchange. First, a halogen atom, such as bromine, is attached to the desired position on the ring system. With the use of special organometallic reagents--compounds with at least one metal-carbon bond--the Br atom can be exchanged for a metal atom, such as magnesium. The Mg atom can then easily be replaced by the desired substituent.
Interestingly, the use of alkali alkoxides in conjunction with the organometallic reagents causes synergistic effects; that is, increased reactivity and altered reactivity profiles. In this manner, lithium alkoxides (LiOR) activate the organo-magnesium reagent sBu(2)Mg (di-sec-butylmagnesium), allowing for an Mg/Br exchange with bromine-containing aromatics.
A team led by Eva Hevia at the University of Bern (Switzerland) has now taken a closer look at this type of reaction, using various methods to trap and analyze the organometallic intermediates that are formed. "We have found a complex equilibrium between various bimetallic species," says Hevia. "The key components are two different intermediates of the Br/Mg exchange that depend on the substitution pattern of the aromatic substrate."
Detailed NMR spectroscopic studies showed that the heart of the reaction is a novel version of the Schlenk equilibrium between bimetallic intermediates, lithium magnesiates, which have different sets of ligands and different Li:Mg ratios. Surprisingly, the in situ generation of an alkyl-rich lithium magnesiate is revealed as the active species of the Mg/Br exchange.
"Our insights advance our understanding of the modus operandi of these fascinating bimetallic systems," states Hevia, "which could pave new paths toward new exciting synthetic applications."
###
About the Author
Originally from Gijon (Spain), Dr. Eva Hevia is a Professor of Inorganic Chemistry at the University of Bern (Switzerland). Research in her group focuses on polar organometallic chemistry at the crossroads of inorganic, organic, and green chemistry with a special emphasis on mechanistic understanding. She is a Fellow of the European Academy of Sciences and her research has been recognized with several awards; e.g., by the British and Spanish chemical societies (RSC, RSEQ)
Journal
Angewandte Chemie International Edition