Issue 8, 2012

New method for C–H arylation/alkylation at α-position of cyclic aliphatic ethers by iron-oxide mediated reaction

Abstract

We report a new and efficient iron oxide catalyzed cross-coupling reaction between organometallic species such as alkyl/arylmagnesium halides or organolithium species and α-hydrogen bearing cyclic unbranched and branched aliphatic ethers via activation of C(sp3)–H. In the presence of 1 mol% of iron oxide, five and six membered unbranched cyclic ethers such as tetrahydrofuran and tetrahydropyran gave good to excellent yields of cross-coupled products. Whereas, in case of branched ether such as 2-methyltetrahydrofuran, it was observed that the arylation occurred at both the sides and gave moderate yields of a mixture of regioisomers. Among the organometallic species used, alkyl organometallic reagents gave less yields as compared to aryl organometallics.

Graphical abstract: New method for C–H arylation/alkylation at α-position of cyclic aliphatic ethers by iron-oxide mediated reaction

Supplementary files

Article information

Article type
Paper
Submitted
30 Sep 2011
Accepted
16 Nov 2011
First published
06 Jan 2012

Org. Biomol. Chem., 2012,10, 1587-1597

New method for C–H arylation/alkylation at α-position of cyclic aliphatic ethers by iron-oxide mediated reaction

P. P. Singh, S. Gudup, H. Aruri, U. Singh, S. Ambala, M. Yadav, S. D. Sawant and R. A. Vishwakarma, Org. Biomol. Chem., 2012, 10, 1587 DOI: 10.1039/C1OB06660A

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