International Journal of Molecular Sciences 2012-01-01

Improved synthesis of 5-substituted 1H-tetrazoles via the [3+2] cycloaddition of nitriles and sodium azide catalyzed by silica sulfuric acid.

Zhenting Du, Changmei Si, Youqiang Li, Yin Wang, Jing Lu

Index: Int. J. Mol. Sci. 13(4) , 4696-703, (2012)

Full Text: HTML

Abstract

A silica supported sulfuric acid catalyzed [3+2] cycloaddition of nitriles and sodium azide to form 5-substituted 1H-tetrazoles is described. The protocol can provide a series of 5-substituted 1H-tetrazoles using silica sulfuric acid from nitriles and sodium azide in DMF in 72%-95% yield.


Related Compounds

Related Articles:

Copper-Catalyzed C-Arylation and Denitrogenation of Tetrazoles: Domino Synthesis of 1, 3-Diaminoisoquinoline Derivatives. Shi L, et al.

[Adv. Synth. Catal. 355(6) , 1177-84, (2013)]

More Articles...