| نویسندگان | سعیده اسدیان,محسن مرادیان,جواد صفری |
| نشریه | chemistryopen |
| شماره صفحات | 1 |
| شماره مجلد | 15 |
| ضریب تاثیر (IF) | ثبت نشده |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2026-01-28 |
| رتبه نشریه | علمی - پژوهشی |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | JCR |
| کلید واژه ها | 1, 8, dioxodecahydroacridines | anionic micelles | green chemistry | nanoreactor |
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چکیده مقاله
In this article, a new anionic surfactant was prepared through a one-pot reaction of stearoyl chloride and benzimidazole with aluminum
chloride under reflux conditions. Its structure was confirmed by 1H and 13C Nuclear magnetic resonance (NMR) analysis
and Fourier transform infrared spectroscopy. The efficacy of the synthesized surfactant system was evaluated in the synthesis of
1,8-dioxodecahydroacridines through a three-component reaction involving aniline, 5,5-dimethylcyclohexan-1,3-dione, and aromatic
aldehydes. It was demonstrated that with a 0.2 g amount of synthesized surfactant 1,3-distearoyl-1H-benzo[d]imidazolium
chloride (DSBimCl), reaction rates could be significantly increased, and the yield in water as solvent without any co-catalyst reached
96%. Additionally, the method is ecofriendly, minimizing the use of harmful organic solvents and facilitating efficient catalytic
processes that are not achievable with traditional organic solvents.