Reaction of N-alkyl-N′-(trimethylsilyl)carbodiimides with nitrating agents. The synthesis of N-(tert-butyl)-N′-nitrocarbodiimide
- 作者: Churakov A.M.1, Ioffe S.L.1, Voronin A.A.1, Tartakovsky V.A.1
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隶属关系:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- 期: 卷 67, 编号 1 (2018)
- 页面: 56-60
- 栏目: Article
- URL: https://bakhtiniada.ru/1066-5285/article/view/241906
- DOI: https://doi.org/10.1007/s11172-018-2037-3
- ID: 241906
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详细
Reaction of N-Alk-N′-(trimethylsilyl)carbodiimides (Alk = Me, But) with nitrating agents (N2O5, (NO2)2SiF6) affords alkyl(nitro)cyanamides and N-alkyl-N′-nitrocarbodiimides. The product ratio depends on the reaction conditions. N-(tert-butyl)-N′-nitrocarbodiimide can be obtained in almost pure form. This compound is stable at temperatures below 10 °C. Its structure was confirmed by 1Н, 13C, and 14N NMR. The reaction of N-(tert-butyl)-N′-nitrocarbodiimide with amines provides a new route to N-alkyl(aryl)-substituted N′-(tert-butyl)-N″-nitroguanidines.
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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