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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Main Authors: Fengli Xin, Chunhua Du, Gongjia Lan, Zhuanping Wu
Format: Article
Language:English
Published: Hindawi Limited 2013-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2013/895892
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spelling 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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