Synthesis of Imidazolium and Benzimidazolium Triiodides
- 作者: Shagun L.G.1, Dorofeev I.A.1, Zhilitskaya L.V.1, Yarosh N.O.1, Larina L.I.1
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隶属关系:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- 期: 卷 55, 编号 7 (2019)
- 页面: 983-987
- 栏目: Article
- URL: https://journals.rcsi.science/1070-4280/article/view/220876
- DOI: https://doi.org/10.1134/S107042801907011X
- ID: 220876
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详细
1,3-(Di)acetonylimidazolium and -benzimidazolium triiodides were synthesized in a one-pot fashion by reactions of imidazole, 3-(1H-imidazol-4-yl)prop-2-enoic acid, benzimidazole, benzimidazol-2-amine, and 2-ethylbenzimidazole with 1-iodopropan-2-one and molecular iodine under solvent-free conditions in the absence of a base and catalyst at room temperature. The reaction of 1H-benzimidazole-2-thiol with 1-iodopropan-2-one and iodine afforded 2-(2-oxopropylsulfanyl)imidazolium triiodide. The reaction direction and yield did not change when 2-iodo-1-(thiophen-2-yl)ethanone was used instead of 1-iodopropan-2-one.
作者简介
L. Shagun
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, Irkutsk
I. Dorofeev
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, Irkutsk
L. Zhilitskaya
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
编辑信件的主要联系方式.
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, Irkutsk
N. Yarosh
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, Irkutsk
L. Larina
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: lara_zhilitskaya@irioch.irk.ru
俄罗斯联邦, Irkutsk
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