Synthesis, Properties, and Hydroboration Activity of the Highly Electrophilic Borane Bis(pentafluorophenyl)borane, HB(C6F5)21

作者：Daniel J. Parks, Warren E. Piers, Glenn P. A. Yap · 发表于：Organometallics · 年份：1998 · DOI：10.1021/om980673e · 被引用次数：526 · 研究领域：Organoboron and organosilicon chemistry、Boron Compounds in Chemistry、Catalytic Cross-Coupling Reactions

Two reliable and efficient routes to bis(pentafluorophenyl)borane, 1, are described. A three-step procedure uses the −C 6 F 5 transfer agent Me 2 Sn(C 6 F 5 ) 2 to produce the chloroborane ClB(C 6 F 5 ) 2, which is subsequently converted to 1 by treatment with a silane, and proceeds with an overall yield of 62%. Alternatively, 1 can be made in 69% yield from B(C 6 F 5 ) 3 and Et 3 SiH by heating the two reagents at 60 °C for 3 days in benzene. Borane 1 is dimeric in the solid state, as determined by X-ray crystallographic analysis. However, in aromatic solvents, detectable amounts of monomeric borane are present (ratio of dimer:monomer ≈4.5:1). The ease of dimer dissociation to monomer coupled with the high electrophilicity of the borane makes 1 a very reactive hydroboration reagent in aromatic solvents. Hydroborations do not proceed in donor solvents such as tetrahydrofuran. A survey of a variety of olefin and alkyne substrates shows that 1 hydroborates with comparable regio- and chemoselectivities to commonly used reagents such as 9-BBN, but at a much faster rate. A second unique feature of the reagent is the facility with which boryl migration takes place in the products of olefin hydroboration. This property can be used to access thermodynamic products of hydroboration where other reagents give diastereomeric kinetic products. Alkynes can be selectively monohydroborated; terminal alkyne substrates will react with a second equivalent of 1, while internal alkynes are immune...