Double acylation product in the snсl4-promoted reaction of 4,5-dichlorocyclopent-4-en-1,3-dione with 1,3,5-trimethoxybenzene
- Authors: Egorov V.A.1, Khasanova L.S.1, Gimalova F.A.1, Miftakhov M.S.1
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Affiliations:
- Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
- Issue: Vol 59, No 8 (2023)
- Pages: 1096-1099
- Section: Articles
- URL: https://aspvestnik.ru/0514-7492/article/view/666225
- DOI: https://doi.org/10.31857/S0514749223080128
- EDN: https://elibrary.ru/JQXXSN
- ID: 666225
Cite item
Abstract
The interaction of 4,5-dichlorocyclopent-4-en-1,3-dione with 1,3,5-trimethoxybenzene under Friedel-Crafts reaction conditions along with the expected 5-(2,4,6-trimethoxyphenyl)-4-chlorocyclopent-4-ene-1,3-dione obtained disubstituted product - 3,4-bis-(2,4,6-trimethoxyphenyl)-2-chlorocyclopent-2-en-1-one.
About the authors
V. A. Egorov
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
L. S. Khasanova
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
F. A. Gimalova
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
Email: fangim@anrb.ru
M. S. Miftakhov
Ufa Institute of Chemistry, Ufa Federal Research Center of the Russian Academy of Sciences
References
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- Egorov V.A., Khasanova L.S., Gimalova F.A., Lobov A.N., Ishmetova D.V., Vakhitov V.A., Miftakhov M.S. Mendeleev Commun. 2022, 32, 183-185. doi: 10.1016/j.mencom.2022.03.010
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