Issue 1, 2020

An umpolung reaction of α-iminonitriles and its application to the synthesis of aminomalononitriles

Abstract

An umpolung N-alkylation reaction of α-iminonitriles with Grignard reagents affords the corresponding N-alkylated α-aminonitriles in good yields. Subsequent oxidation and cyanation of the N-alkylated products proceeds effectively to give aminomalononitriles in good yields, and the presence of dichlorodimethylsilane as an additive is crucial for obtaining the optimum yield. Furthermore, an electrophilic addition reaction of the intermediate halomagnesium vinylideneamide is shown to give the alkylated and acylated products in good yields.

Graphical abstract: An umpolung reaction of α-iminonitriles and its application to the synthesis of aminomalononitriles

Supplementary files

Article information

Article type
Paper
Submitted
11 Oct 2019
Accepted
20 Nov 2019
First published
20 Nov 2019

New J. Chem., 2020,44, 152-161

An umpolung reaction of α-iminonitriles and its application to the synthesis of aminomalononitriles

M. Shimizu, Y. Furukawa, I. Mizota and Y. Zhu, New J. Chem., 2020, 44, 152 DOI: 10.1039/C9NJ05114G

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