Chin. J. Org. Chem. ›› 2014, Vol. 34 ›› Issue (11): 2272-2278.DOI: 10.6023/cjoc201406021 Previous Articles     Next Articles


李婉a, 唐建刚a, 胡艾希a, 叶姣a, 杨子辉a, 欧晓明b   

  1. a 湖南大学化学化工学院 长沙 410082;
    b 湖南化工研究院 长沙 410007
  • 收稿日期:2014-06-15 修回日期:2014-07-07 发布日期:2014-07-15
  • 通讯作者: 胡艾希,
  • 基金资助:


Synthesis and Fungicidal Activity of 2-(2,2-Dimethyl-2,3-dihydro-benzofuran-5-yl)-2-(1,2,4-triazole-1-methyl)-1,3-dioxolane

Li Wana, Tang Jianganga, Hu Aixia, Ye Jiaoa, Yang Zihuia, Ou Xiaomingb   

  1. a Colleage of Chemistry and Chemical Engineering, Hunan University, Changsha 410082;
    b Hunan Research Institute of Chemical Industry, Changsha 410007
  • Received:2014-06-15 Revised:2014-07-07 Published:2014-07-15
  • Supported by:

    Project supported by the State Commission of Science Technology of China (No.2011BAE06B01).

Benzofuran and 1,2,4-triazole have been rewarded with much priority for their broad spectrum of biological activities, especially in the agricultural field. In this specific domain, they have always been used as fungicides, pesticide and plant growth regulators etc. Consequently, a series of new compounds containing 1,2,4-triazole, 1,3-dioxolane and benzofuran moieties were designed and synthesized. 1-(2,2-Dimethyl-2,3-dihydrobenzofuran-5-yl)ethanone (4a) were prepared from 1-(4-hydroxyphenyl)ethanone in three steps. Subsequently, 2-(2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-2-(1,2,4-triazol-1-methyl)-1,3-dioxolane (1a~1l) were synthesized from compounds 4a~4c. All compounds were verified by NMR and elemental analysis. Additionally, their fungicidal activities were evaluated against 7 kinds of crop fungus. The compounds 1a, 1b, 1e, 1f, 1g and 1l had relatively good inhibitory activity against Sclerotonia sclerotiorum, and the inhibitory rate were above 70% at 25 mg/L. Meanwhile, compounds 1a and 1b possessed potent inhibitory activity (80%) against Blumeria graminis at 500 mg/L.

Key words: 1,3-dioxolane, 2,2-dimethyl-2,3-dihydrobenzofuran, 1,2,4-triazole, fungicidal activity