Preparation of Functionalized Aryl, Heteroaryl, and Benzylic Potassium Organometallics Using Potassium Diisopropylamide in Continuous Flow

被引:14
|
作者
Harenberg, Johannes H. [1 ]
Weidmann, Niels [1 ]
Knochel, Paul [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Dept Chem, Butenandtstr 5-13,Haus F, D-81377 Munich, Germany
关键词
arenes; flow chemistry; heteroarenes; lateral metalation; potassium; DIRECTED ORTHO-METALATION; SODIUM DIISOPROPYLAMIDE; ORGANOLITHIUM COMPOUNDS; ALKALI-METALS; STRONG BASES; LITHIUM; REARRANGEMENT; DERIVATIVES; ALKOXIDES; REAGENTS;
D O I
10.1002/anie.202003392
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the preparation of lithium-salt-free KDA (potassium diisopropylamide; 0.6 m in hexane) complexed with TMEDA (N,N,N ',N '-tetramethylethylenediamine) and its use for the flow-metalation of (hetero)arenes between -78 degrees C and 25 degrees C with reaction times between 0.2 s and 24 s and a combined flow rate of 10 mL min(-1) using a commercial flow setup. The resulting potassium organometallics react instantaneously with various electrophiles, such as ketones, aldehydes, alkyl and allylic halides, disulfides, Weinreb amides, and Me3SiCl, affording functionalized (hetero)arenes in high yields. This flow procedure is successfully extended to the lateral metalation of methyl-substituted arenes and heteroaromatics, resulting in the formation of various benzylic potassium organometallics. A metalation scale-up was possible without further optimization.
引用
收藏
页码:12321 / 12325
页数:5
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