Issue 17, 2012

Iron(ii) catalyzed dehydrative etherification of alcohols: a convenient route to ferrocenylmethanol-ethers

Abstract

The iron complex [Fp][OTf] (Fp+[double bond, length as m-dash][Fe(CO)2(Cp)]+, OTf[double bond, length as m-dash]SO3CF3) was found to act as efficient catalyst for the dehydrative etherification of ferrocenylmethanol [HOCH2–Fc] with a variety of alcohols (ROH), providing a valuable route for the formation of ferrocenylmethanol-ethers [ROCH2–Fc]. The complex [Fp][OTf] also catalyzes etherification of propargyl alcohols with other alcohols. The advantages of the method are associated with the use of a non toxic and easily available transition metal as catalyst, and the dehydrative synthetic approach, which produces water as the only by-product.

Graphical abstract: Iron(ii) catalyzed dehydrative etherification of alcohols: a convenient route to ferrocenylmethanol-ethers

Supplementary files

Article information

Article type
Paper
Submitted
18 Apr 2012
Accepted
18 May 2012
First published
21 May 2012

RSC Adv., 2012,2, 6810-6816

Iron(II) catalyzed dehydrative etherification of alcohols: a convenient route to ferrocenylmethanol-ethers

L. Busetto, R. Mazzoni, M. Salmi, S. Zacchini and V. Zanotti, RSC Adv., 2012, 2, 6810 DOI: 10.1039/C2RA20708G

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