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Kinetics and Mechanism of Certain Acetylation Reactions with Acetamide/Oxychloride in Acetonitrile under VilsmeierHaack Conditions

✍ Scribed by Marri Venkateswarlu; Mukka Satish Kumar; Soma Ramgopal; Kamatala Chinna Rajanna; Utkoor Umesh Kumar; Kusampally Uppalaiah; Pondichery Kuppuswamy Saiprakash


Publisher
John Wiley and Sons
Year
2011
Tongue
German
Weight
354 KB
Volume
94
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

VilsmeierHaack (VH) acetylation reactions with benzaldehydes or acetophenones in MeCN followed second‐order kinetics and afforded acetyl derivatives under kinetic conditions, irrespective of the nature of the oxychloride (SOCl~2~ or POCl~3~) used for the preparation of the VH reagent along with acetamide. The present finding contributes to the understanding of the nature of the reactive species of the VH reagent as well as of the acetylation mechanism.


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