Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination

Nitration of N-acetyl anilides using a simple combination of AgNO3 and K2S2O8 as a stable nitro source and an oxidant, respectively, was explored. The reaction was practical to operate and proceeded under considerably mild reaction conditions (reflux in acetonitrile) within acceptable reaction time...

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Main Author: Sanjeam H.
Other Authors: Mahidol University
Format: Article
Published: 2023
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/84219
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spelling th-mahidol.842192023-06-18T23:59:36Z Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination Sanjeam H. Mahidol University Chemistry Nitration of N-acetyl anilides using a simple combination of AgNO3 and K2S2O8 as a stable nitro source and an oxidant, respectively, was explored. The reaction was practical to operate and proceeded under considerably mild reaction conditions (reflux in acetonitrile) within acceptable reaction time (6 h). The para-substituted N-acetyl anilides gave only ortho-nitrated products in moderate to good yields (30–63% yields). The ortho-, meta-, or non-substituted N-acetyl anilides gave a mixture of nitrated products (30–72% combined yields) with preferentially at the para- over the ortho-position (ortho:para; 1.0:1.1–1.0:2.8). 2023-06-18T16:59:36Z 2023-06-18T16:59:36Z 2022-01-01 Article Synthetic Communications Vol.52 No.9-10 (2022) , 1279-1289 10.1080/00397911.2022.2081924 15322432 00397911 2-s2.0-85131563495 https://repository.li.mahidol.ac.th/handle/123456789/84219 SCOPUS
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Chemistry
spellingShingle Chemistry
Sanjeam H.
Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
description Nitration of N-acetyl anilides using a simple combination of AgNO3 and K2S2O8 as a stable nitro source and an oxidant, respectively, was explored. The reaction was practical to operate and proceeded under considerably mild reaction conditions (reflux in acetonitrile) within acceptable reaction time (6 h). The para-substituted N-acetyl anilides gave only ortho-nitrated products in moderate to good yields (30–63% yields). The ortho-, meta-, or non-substituted N-acetyl anilides gave a mixture of nitrated products (30–72% combined yields) with preferentially at the para- over the ortho-position (ortho:para; 1.0:1.1–1.0:2.8).
author2 Mahidol University
author_facet Mahidol University
Sanjeam H.
format Article
author Sanjeam H.
author_sort Sanjeam H.
title Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
title_short Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
title_full Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
title_fullStr Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
title_full_unstemmed Nitration of N-acetyl anilides using silver(I) nitrate/persulfate combination
title_sort nitration of n-acetyl anilides using silver(i) nitrate/persulfate combination
publishDate 2023
url https://repository.li.mahidol.ac.th/handle/123456789/84219
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