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Silanol Salt for Deprotection Reactions and Cross-coupling Reactions
Potassium trimethylsiloxide (1) is used not only in the dealkylation of esters1,2) but also as a base in Suzuki-Miyaura cross-coupling,3) in the disconnection of carbon-silicon bond4) and hydrolysis of nitriles.5) It is considered that the dealkylation of esters using 1 mainly proceeds through a nucleophilic attack of the silanolate anion and can be performed under milder conditions when compared to other reagents with the same reaction mechanism. In Suzuki-Miyaura cross-coupling, the reaction can proceed rapidly under anhydrous conditions. Moreover, the protodesilylation reaction requires only catalytic amount of 1 and the sp3, sp2 and sp carbon-silicon bonds are easily disconnected. In this way, a number of reports are increasing recently due to the wide variety of application of 1.
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References
- 1) Metal silanolates: organic soluble equivalents for O−2
- 2) Scope and Limitations of Sodium and Potassium Trimethylsilanolate as Reagents for Conversion of Esters to Carboxylic Acids
- 3) Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki−Miyaura Cross-Coupling of Boronic Esters
- 4) An Additive-Free, Base-Catalyzed Protodesilylation of Organosilanes
- 5) Potassium trimethylsilanolate mediated hydrolysis of nitriles to primary amides