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An Updated Synthesis of the Diazo-Transfer Reagent Imidazole-1-sulfonyl Azide Hydrogen Sulfate
Author(s) -
Garrett T. Potter,
Gordon C. Jayson,
Gavin J. Miller,
John M. Gardiner
Publication year - 2016
Publication title -
the journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.2
H-Index - 228
eISSN - 1520-6904
pISSN - 0022-3263
DOI - 10.1021/acs.joc.6b00177
Subject(s) - diazo , reagent , chemistry , sulfonyl , azide , salt (chemistry) , diazonium compounds , sulfate , combinatorial chemistry , inorganic chemistry , organic chemistry , alkyl
Imidazole-1-sulfonyl azide and salts thereof are valuable reagents for diazo-transfer reactions, most particularly conversion of primary amines to azides. The parent reagent and its HCl salt present stability and detonation risks, but the hydrogen sulfate salt is significantly more stable. An updated procedure for the large-scale synthesis of this salt avoids isolation or concentration of the parent compound or HCl salt and will facilitate the use of hydrogen sulfate salt as the reagent of choice for diazo transfer.

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