A simple and effective synthesis of aryl azides via arenediazonium tosylates

Ksenia V. Kutonova, Marina E. Trusova, Pavels Postnikov, Victor D. Filimonov, Joseph Parello

Research output: Contribution to journal › Article

Abstract

Aromatic azides are formed in high yield from arenediazonium tosylates and sodium azide in water at room temperature or from aromatic amines via diazotization in the presence of p-TsOH Besides being experimentally simple, these methods do not require any metal catalysis and provide clean products without purification.

Original language	English
Article number	7106
Pages (from-to)	2706-2710
Number of pages	5
Journal	Synthesis (Germany)
Volume	45
Issue number	19
DOIs	https://doi.org/10.1055/s-0033-1339648
Publication status	Published - 9 Oct 2013

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Keywords

aqueous medium
aromatic amines
diazotization
p -TsOH
sodium azide

ASJC Scopus subject areas

Catalysis
Organic Chemistry

Cite this

Kutonova, K. V., Trusova, M. E., Postnikov, P., Filimonov, V. D., & Parello, J. (2013). A simple and effective synthesis of aryl azides via arenediazonium tosylates. Synthesis (Germany), 45(19), 2706-2710. [7106]. https://doi.org/10.1055/s-0033-1339648

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Access to Document

10.1055/s-0033-1339648