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Synthesis 2015; 47(12): 1749-1760
DOI: 10.1055/s-0034-1380155
DOI: 10.1055/s-0034-1380155
paper
Synthesis of Ethers from Carbonyl Compounds by Reductive Etherification Catalyzed by Iron(III) and Silyl Chloride
Further Information
Publication History
Received: 07 November 2014
Accepted after revision: 15 January 2015
Publication Date:
18 February 2015 (online)
Abstract
A simple iron- and silyl chloride catalyzed method for the preparation of symmetrical and nonsymmetrical ethers is presented. Various aldehydes and ketones were reductively etherified by using triethylsilane as a reducing agent in the presence of 2 mol% of iron(III) oxo acetate and 8 mol% of chloro(trimethyl)silane. The reactions can be carried out at ambient temperatures and pressures with ethyl acetate as the solvent.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1380155. Included are details on catalyst preparation and characterization and copies of NMR and GC chromatograms of the isolated products.
- Supporting Information
-
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