Silica Sulfuric Acid as an Efficient Reagent for Bamberger Rearrangement of Phenyl Hydroxylamine Derivatives in Solvent-Free Conditions
Corresponding Author(s) : RASHID BADRI
rashidbadri@yahoo.com
Asian Journal of Chemistry,
Vol. 19 No. 6 (2007): Vol 19 Issue 6
Abstract
Phenyl hydroxylamines undergo Bamberger rearrangement in the presence of silica sulfuric acid under solvent-free conditions to afford the corresponding 4-amino phenol derivatives in high yields.
Keywords
Phenyl hydroxylamines
Silica sulfuric
Non-solvent
Bamberger rearrangement
BADRI, R., & REZA SHUSHIZADEH, M. (2010). Silica Sulfuric Acid as an Efficient Reagent for Bamberger Rearrangement of Phenyl Hydroxylamine Derivatives in Solvent-Free Conditions. Asian Journal of Chemistry, 19(6), 4661–4664. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/19982
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