For the first time, the direct synthesis of 1-methyl-phosphininium salts has been achieved by reacting aromatic λ,σ-phosphinines with the readily available dimethyl chloronium salt [(CH)Cl][Al(OTeF)]. The remarkably high electrophilicity of the alkylation reagent in combination with the weakly coordinating pentafluoro-orthotelluratoaluminate anion offers excellent conditions for this one-step approach. Our simple and quantitative access to 1-methyl-phosphininium salts will pave the way to explore the chemistry of such reactive species in more detail.
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http://dx.doi.org/10.1039/d1cc03892c | DOI Listing |
Chem Commun (Camb)
September 2021
Institut für Chemie und Biochemie, Freie Universität Berlin, Fabeckstrasse 34/36, Berlin 14195, Germany.
For the first time, the direct synthesis of 1-methyl-phosphininium salts has been achieved by reacting aromatic λ,σ-phosphinines with the readily available dimethyl chloronium salt [(CH)Cl][Al(OTeF)]. The remarkably high electrophilicity of the alkylation reagent in combination with the weakly coordinating pentafluoro-orthotelluratoaluminate anion offers excellent conditions for this one-step approach. Our simple and quantitative access to 1-methyl-phosphininium salts will pave the way to explore the chemistry of such reactive species in more detail.
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