Synthesis of Hydrazones of Stobbe Acid and its Rearranged Products
Corresponding Author(s) : M.A. Dave
sandhya@somaiya.com
Asian Journal of Chemistry,
Vol. 17 No. 2 (2005): Vol 17 Issue 2
Abstract
Stobbe anhydride (I and II) was condensed with diazonium salts of various atomatic amines to form hydrazones or dyes [I and II (a-c)] which were further treated with nucleophiles like 10% NaOH and NaBH4 to give various pyrazolinone [I and II (d-f)], [I and II (g-i)] and cyclic imide [I and II (j-l)] derivatives.
Keywords
Stobbe acid anhydride
Nuclephiles
Jacob, J., Dave, M., & Parashar, S. (2016). Synthesis of Hydrazones of Stobbe Acid and its Rearranged Products. Asian Journal of Chemistry, 17(2), 1315–1318. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/14348
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