Synthesis of N-nitro-N′-(trimethylsilyl)carbodiimide


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详细

Nitration of N,N′-bis(trimethylsilyl)carbodiimide with N2O5 or (NO2)2SiF6 afforded N-nitro-N´-(trimethylsilyl)carbodiimide, the first representative of N-nitro carbodiimides. Its further nitration led to the release of CO2, which is presumably formed in the course of N,N´-dinitrocarbodiimide decomposition. The reactions of N-nitro-N´-(trimethylsilyl)carbodiimide with nucleophiles take place both at the tri methylsilyl group (for example, with NH3) to give nitrocyanamide salts and at the carbodiimide C atom (for example, with Et2NH) to give the corresponding nitroguan idines.

作者简介

A. Churakov

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

编辑信件的主要联系方式.
Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

S. Ioffe

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

A. Voronin

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

V. Tartakovsky

N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Email: churakov@ioc.ac.ru
俄罗斯联邦, 47 Leninsky prosp., Moscow, 119991

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