Staudinger Reaction as a Way Out To Avoid Cyclization in the Reaction of Silylated Dichloro(hydrazino)phosphane with Trimethylsilyl Azide
Axel Schulz, Alexander Villinger
Abstract
Axel Schulz, Alexander Villinger
Abstract
Abstract Reaction of dichloro‐N,N′,N′‐[tris(trimethylsilyl)]hydrazinophosphane (1) with Me3SiN3 leads after an initial chlorine/azide exchange in a Staudinger reaction to a new phosphorus azide. The in situ formed phosphoranimine reacts with GaCl3 by Me3SiCl elimination, resulting in a phosphoranimino–dichlorogallane, which dimerizes to a Ga2N2‐four‐membered ring. The overall reaction at ambient temperature represents a fast and clean high‐yielding reaction (reaction time 2 h). The dimer of the formed azido–phosphoranimino–dichlorogallane was fully characterized and shown to be stable to temperatures above 103 °C.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
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Abstract Reaction of dichloro‐N,N′,N′‐[tris(trimethylsilyl)]hydrazinophosphane (1) with Me3SiN3 leads after an initial chlorine/azide exchange in a Staudinger reaction to a new phosphorus azide. The in situ formed phosphoranimine reacts with GaCl3 by Me3SiCl elimination, resulting in a phosphoranimino–dichlorogallane, which dimerizes to a Ga2N2‐four‐membered ring. The overall reaction at ambient temperature represents a fast and clean high‐yielding reaction (reaction time 2 h). The dimer of the formed azido–phosphoranimino–dichlorogallane was fully characterized and shown to be stable to temperatures above 103 °C.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Key concepts: Chemistry, Azide, Trimethylsilyl azide, Trimethylsilyl, Staudinger reaction, Medicinal chemistry, Tris, Dimer