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DOI: 10.1055/a-2735-9141
Facile Synthesis of 1H-Indoliums via Silica Gel-Assisted Silver-Catalyzed Intramolecular Hydroammoniumation of ortho-Alkynylanilines
Authors
Supported by: Institute of Pharmaceutical Life Sciences, Aichi Gakuin University
Funding Information This research was supported by a research grant from Institute of Pharmaceutical Life Sciences, Aichi Gakuin University.

Abstract
1H-Indoliums, a class of cationic heterocycles, with potential industrial applications have been used as components in capacitors. In this study, we describe a facile method for the synthesis of indoliums using silica gel-assisted silver-catalyzed intramolecular hydroammoniumation of ortho-alkynylanilines. The cyclization of alkynylanilines in the presence of AgOTf (5 mol%), LiOTf (1 equiv.), and SiO2 [SiO2/AgOTf (w/w: 199/1)] in CH2Cl2 at room temperature under aerobic conditions afforded indoliums in good-to-excellent yields. This reaction is an effective and novel method, in which the 5-endo-dig cyclization reaction to obtain indoliums is promoted only by the addition of SiO2 in the presence of a silver catalyst. This novel methodology offers a practical and effective route for the synthesis of indoliums under mild conditions.
Publication History
Received: 23 August 2025
Accepted after revision: 17 October 2025
Article published online:
20 November 2025
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References
- 1a Biswas S, Pal A, Pal T. RSC Adv 2020; 10: 35449
- 1b Chanu LV, Singh OM. J Heterocycl chem 2021; 58: 2207
- 1c Zhang M, Yang J-H. ChemistrySelect 2022; 7: e202200013
- 2a Williams CM, Mander LN. Tetrahedron 2001; 57: 425
- 2b Mander LN, Williams CM. Tetrahedron 2016; 72: 1133
- 3 Machida K, Yoshida Y, Igawa K, Tomooka K. Chem Lett 2018; 47: 186
- 4a Marshall JA, Sehon CA. J Org Chem 1995; 60: 5966
- 4b Marshall JA, Hinkle KW. J Org Chem 1997; 62: 5989
- 4c van Esseveldt BCJ, Vervoort PWH, van Delft FL, Rutjes FPJT. J Org Chem 2005; 70: 1791
- 4d Hayes SJ, Knight DW, Menzies MD, O’Halloran M, Tan W-F. Tetrahedron Lett 2007; 48: 7709
- 4e Knight D, Proctor A, Clough J. Synlett 2010; 628
- 4f Sharland CM, Singkhonrat J, NajeebUllah M, Hayes SJ, Knight DW, Dunford DG. Tetrahedron Lett 2011; 52: 2320
- 4g Dunford DG, Knight DW. Tetrahedron Lett 2016; 57: 2746
- 4h Clarke AK, James MJ, O’Brien P, Taylor RJK, Unsworth WP. Angew Chem Int Ed 2016; 55: 13798
- 6 Hinman RL, Lang J. J Org Chem 1964; 29: 1449
- 7 Voss T, Chen C, Kehr G, Nauha E, Erker G, Stephan DW. Chem Eur J 2010; 16: 3005
- 8 Zeng X, Kinjo R, Donnadieu B, Bertrand G. Angew Chem Int Ed 2010; 49: 942
- 10a Yue D, Yao T, Larock RC. J Org Chem 2006; 71: 62
- 10b Ge G, Huang X, Ding C, Li H, Wan S, Hou X. Chin J Chem 2014; 32: 727
- 10c Niu S-L, Hu J, He K, Chen Y-C, Xiao Q. Org Lett 2019; 21: 4250
- 10d Yang F, Hu Y, Wang L, Wu M, Yuan X, Liu Z, Li X, Wang Z, Zheng H. Asian J Org Chem 2022; 11: e202100750
- 10e Ohmura T, Yagi K, Torigoe T, Suginome M. Synthesis 2021; 53: 3057