Aromatic C-acylation of Phenols by using Acid and Acid Anhydride in Presence of Lewis Acid Catalyst

Journal Title: American Journal of PharmTech Research - Year 2018, Vol 8, Issue 0

Abstract

Ring acylations of aromatic substances are very difficult to achieve to a great extent. Nencki reaction has attempted on mono to poly hydroxy and substituted phenols have good results. Reactions are using solely acetic acid, acetic anhydride and adipic acid or mixture of acid and anhydride resulting complete consumption of phenols. The use Lewis acid freshly fused ZnCl2 is best suitable catalyst compare to others. The essential data on phenols acylation has been studied and described as below.

Authors and Affiliations

Mahendra Sawant

Keywords

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Aromatic C-acylation of Phenols by using Acid and Acid Anhydride in Presence of Lewis Acid Catalyst

Ring acylations of aromatic substances are very difficult to achieve to a great extent. Nencki reaction has attempted on mono to poly hydroxy and substituted phenols have good results. Reactions are using solely acetic a...

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  • EP ID EP619771
  • DOI 10.21276/ajptr.2018.08.05.12
  • Views 155
  • Downloads 0

How To Cite

Mahendra Sawant (2018). Aromatic C-acylation of Phenols by using Acid and Acid Anhydride in Presence of Lewis Acid Catalyst. American Journal of PharmTech Research, 8(0), 131-139. https://europub.co.uk/articles/-A-619771