Article ID Journal Published Year Pages File Type
1323369 Journal of Organometallic Chemistry 2012 5 Pages PDF
Abstract

An efficient method for the synthesis of α-aminonitriles via one-pot three-component condensation of ketones, amines and potassium hexacyanoferrate(II) using benzoyl chloride as a promoter and PEG-400 as a reaction medium was described. This protocol has the features of use of eco-friendly cyanide source, green reaction medium, high yield, and simple work-up procedure.

Graphical abstractAn efficient method for the synthesis of α-aminonitriles via one-pot three-component condensation of ketones, amines and potassium hexacyanoferrate(II) using benzoyl chloride as a promoter and PEG-400 as a reaction medium was described.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► High yielding synthesis of α-aminonitriles from ketones. ► Eco-friendly cyanide source, K4[Fe(CN)6]. ► Eco-friendly reaction medium, PEG-400. ► An efficient promoter, benzoyl chloride.

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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