Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone
A novel synthetic approach towards 5-fluoro-2-hydroxy butyrophenone is reported. Using 4-fluorophenol as a raw material, the processes of etherification protection, Friedel-Crafts acylation and demethylation provide the target compound under mild conditions. The structure was characterized by the me...
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doaj-4318865737634ca7bb586e79fb8e5e4b2020-11-24T22:36:38ZengHindawi LimitedJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/895892895892Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy ButyrophenoneFengli Xin0Chunhua Du1Gongjia Lan2Zhuanping Wu3College of Chemistry & Pharmacy, Qingdao Agricultural University, Research Center of Agricultural Bionic Engineering & Technology of Shandong Province, Qingdao 266109, ChinaCollege of Chemistry & Pharmacy, Qingdao Agricultural University, Research Center of Agricultural Bionic Engineering & Technology of Shandong Province, Qingdao 266109, ChinaCollege of Chemistry & Pharmacy, Qingdao Agricultural University, Research Center of Agricultural Bionic Engineering & Technology of Shandong Province, Qingdao 266109, ChinaCollege of Chemistry & Pharmacy, Qingdao Agricultural University, Research Center of Agricultural Bionic Engineering & Technology of Shandong Province, Qingdao 266109, ChinaA novel synthetic approach towards 5-fluoro-2-hydroxy butyrophenone is reported. Using 4-fluorophenol as a raw material, the processes of etherification protection, Friedel-Crafts acylation and demethylation provide the target compound under mild conditions. The structure was characterized by the melting point and IR, MS, 1H-NMR, and 13C-NMR spectroscopy. The bioassay results indicate that the target compound exhibits potent antifungal activities against Valsa mali, Coniella dipodiella, and other agricultural plant fungi. The target compound also shows potent herbicidal activities for Lactuca sativa, a dicotyledon, and Echinochloa crus-galli, a monocotyledon. The toxicity regression C50 values of the compound against Valsa mali, Coniothyrium diplodiella, Lactuca sativa seedling, and Echinochloa crusgalli seedling were calculated by SPSS. The Hormesis effect for roots of Echinochloa crusgalli was confirmed.http://dx.doi.org/10.1155/2013/895892 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fengli Xin Chunhua Du Gongjia Lan Zhuanping Wu |
spellingShingle |
Fengli Xin Chunhua Du Gongjia Lan Zhuanping Wu Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone Journal of Chemistry |
author_facet |
Fengli Xin Chunhua Du Gongjia Lan Zhuanping Wu |
author_sort |
Fengli Xin |
title |
Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone |
title_short |
Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone |
title_full |
Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone |
title_fullStr |
Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone |
title_full_unstemmed |
Synthesis, Characterization, and Agricultural Biological Activities of 5-Fluoro-2-hydroxy Butyrophenone |
title_sort |
synthesis, characterization, and agricultural biological activities of 5-fluoro-2-hydroxy butyrophenone |
publisher |
Hindawi Limited |
series |
Journal of Chemistry |
issn |
2090-9063 2090-9071 |
publishDate |
2013-01-01 |
description |
A novel synthetic approach towards 5-fluoro-2-hydroxy butyrophenone is reported. Using 4-fluorophenol as a raw material, the processes of etherification protection, Friedel-Crafts acylation and demethylation provide the target compound under mild conditions. The structure was characterized by the melting point and IR, MS, 1H-NMR, and 13C-NMR spectroscopy. The bioassay results indicate that the target compound exhibits potent antifungal activities against Valsa mali, Coniella dipodiella, and other agricultural plant fungi. The target compound also shows potent herbicidal activities for Lactuca sativa, a dicotyledon, and Echinochloa crus-galli, a monocotyledon. The toxicity regression C50 values of the compound against Valsa mali, Coniothyrium diplodiella, Lactuca sativa seedling, and Echinochloa crusgalli seedling were calculated by SPSS. The Hormesis effect for roots of Echinochloa crusgalli was confirmed. |
url |
http://dx.doi.org/10.1155/2013/895892 |
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