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International Journal of Creative and Open Research in Engineering and Management

A Peer-Reviewed, Open-Access International Journal Supporting Multidisciplinary Research, Digital Publishing Standards, DOI Registration, and Academic Indexing.
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ISSN: 3108-1754 (Online)
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Publication Fee: 599/- INR
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License: CC BY 4.0
Peer Review: Double Blind
Volume 02, Issue 03

Published on: March 2026 2026

CONVERSION OF BENZENE TO BENZANILIDE VIA BECKMANN REARRANGEMENT

Dr. Naimish Kumar Verma

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Plagiarism Passed Peer Reviewed Open Access

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Abstract

Benzanilide (C₆H₅–CO–NH–C₆H₅) is an aromatic amide widely used in pharmaceutical and organic synthesis. A convenient synthetic route involves the Beckmann rearrangement of acetophenone oxime. This study presents a stepwise method starting from benzene, detailing the preparation of acetophenone via Friedel–Crafts acylation, formation of acetophenone oxime, and subsequent rearrangement to benzanilide under acidic conditions.

How to Cite this Paper

Verma, N. K. (2026). Conversion of Benzene to Benzanilide via Beckmann Rearrangement. International Journal of Creative and Open Research in Engineering and Management, <i>02</i>(03). https://doi.org/10.55041/ijcope.v2i3.046

Verma, Naimish. "Conversion of Benzene to Benzanilide via Beckmann Rearrangement." International Journal of Creative and Open Research in Engineering and Management, vol. 02, no. 03, 2026, pp. . doi:https://doi.org/10.55041/ijcope.v2i3.046.

Verma, Naimish. "Conversion of Benzene to Benzanilide via Beckmann Rearrangement." International Journal of Creative and Open Research in Engineering and Management 02, no. 03 (2026). https://doi.org/https://doi.org/10.55041/ijcope.v2i3.046.

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  • All submissions are screened under plagiarism detection.
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  • Peer Review Type: Double-Blind Peer Review
  • Published on: Mar 11 2026
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