In situ Grignard Metalation Method, Part II : Scope of the One‐Pot Synthesis of Organocalcium Compounds

GND
1263590586
ORCID
0000-0002-1131-7703
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena, Humboldtstraße 8, 07743 Jena, Germany
Schüler, Philipp;
GND
129923240X
ORCID
0000-0002-5145-2889
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University Jena, Humboldtstraße 8, 07743 Jena, Germany
Sengupta, Simon;
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry Friedrich Schiller University Jena Humboldtstraße 8 07743 Jena Germany
Koch, Alexander;
GND
1214845193
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry Friedrich Schiller University Jena Humboldtstraße 8 07743 Jena Germany
Görls, Helmar;
GND
141415746
ORCID
0000-0002-6142-7679
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry Friedrich Schiller University Jena Humboldtstraße 8 07743 Jena Germany
Krieck, Sven;
GND
1014223741
ORCID
0000-0002-1520-2401
Zugehörigkeit
Institute of Inorganic and Analytical Chemistry Friedrich Schiller University Jena Humboldtstraße 8 07743 Jena Germany
Westerhausen, Matthias

The in situ Grignard Metalation Method ( i GMM) is a straightforward one‐pot strategy to synthesize alkaline‐earth metal amides in multi‐gram scale with high yields via addition of bromoethane to an ethereal suspension of a primary or secondary amine and magnesium (Part I) or calcium (Part II). This method is highly advantageous because no activation of calcium is required prior to the reaction. Contrary to the magnesium‐based i GMM, there are some limitations, the most conspicuous one is the large influence of steric factors. The preparation of Ca(hmds) 2 succeeds smoothly within a few hours with excellent yields opening the opportunity to prepare large amounts of this reagent. Side reactions and transfer of the i GMM to substituted anilines and N‐heterocycles as well as other H‐acidic substrates such as cyclopentadienes are studied. Bulky amidines cannot be converted directly to calcium amidinates via the i GMM but stoichiometric calciation with Ca(hmds) 2 enables their preparation.

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