期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 28, 期 69, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202202660
关键词
alkali metals; chirality; lithium; potassium; X-ray diffraction
资金
- Fonds der Chemischen Industrie (FCI)
- Projekt DEAL
This article investigates the metalation of N,N-dimethylaminomethylferrocene by superbase and the preparation of enantiomerically pure superbase. Quantum chemical calculations provide insights into the mechanism of substrate-reagent interaction, and a closer look at the reaction site is presented through experimental studies.
The metalation of N,N-dimethylaminomethylferrocene in THF by the superbasic mixture of (BuLi)-Bu-n/(KOBu)-Bu-t proceeds readily at low temperatures to afford a bimetallic Li2K2 aggregate containing ferrocenyl anions and tert-butoxide. Starting from an enantiomerically enriched ortho-lithiated aminomethylferrocene, an enantiomerically pure superbase can be prepared. The molecular compound exhibits superbasic behavior deprotonating N,N-dimethylbenzylamine in the alpha-position and is also capable of deprotonating toluene. Quantum chemical calculations provide insight into the role of the bridging THF molecule to the possible substrate-reagent interaction. In addition, a benzylpotassium alkoxide adduct gives a closer look into the corresponding reaction site of the Lochmann-Schlosser base that is reported herein.
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