Efficient synthesis of ferrocenylenones by Friedel-Crafts acylation with EtAlCl2-Me3Al

Date

2005-01-17

Author

Doğan, Özdemir
ZEYTİNCİ, SERHAT
KOYUNCU, HASAN
BULUT, ADNAN

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Efficient synthesis of ferrocenyl en ones using a Friedel-Crafts acylation reaction is described. Acryloyl, methacryloyl, crotonoyl, cinnamoyl, and beta-methylcrotonoyl chlorides react with ferrocene in the presence of a Lewis acid (EtAlC2 or EtAlCl2-Me3Al) to give the corresponding ferrocenyl en ones (acryloyl, methacryloyl, crotonoyl, cinnamoyl, and methylcrotonoylferrocenes) in good isolated yields. Besides ferrocenylenones, chloroactylferrocene is also synthesised by this method.

Subject Keywords

Ferrocenylenones, Friedel-Crafts acylation, Ethylaluminum dichloride, Lewis acid

URI

https://hdl.handle.net/11511/41976

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY

DOI

https://doi.org/10.1016/j.jorganchem.2004.09.055

Collections

Department of Chemistry, Article

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Citation Formats

Ö. Doğan, S. ZEYTİNCİ, H. KOYUNCU, and A. BULUT, “Efficient synthesis of ferrocenylenones by Friedel-Crafts acylation with EtAlCl2-Me3Al,” JOURNAL OF ORGANOMETALLIC CHEMISTRY, pp. 430–434, 2005, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/41976.