Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1255045 | Chinese Chemical Letters | 2010 | 5 Pages |
Abstract
An efficient and simple method for the preparation of 5-arylamino-1H-tetrazole and 1-aryl-5-amino-1H-tetrazole derivatives is reported using aluminum(III) hydrogensulfate (Al(HSO4)3) as an effective heterogeneous catalyst from secondary arylcyanamides. Generally, when the substitution in arylcyanamide is strongly electron-withdrawing the position of equilibrium would shift toward the isomer of 1-aryl-5-amino-1H-tetrazole (B) and as the electron-donating of substituent increased, the position of equilibrium is shifted toward the isomer of 5-arylamino-1H-tetrazole (A). The present methodology offers several advantages, such as excellent yields, short reaction times, easy work-up and greener conditions.
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Authors
Ferydoon Khamooshi, Ali Reza Modarresi-Alam,