2-(4-Pyridyl)-1,3-di(4-picolyl)imidazolidine

Beyhan Yiğit,İsmail Özdemir,Bekir Çetinkaya,Engin Çetinkaya,Murat Yiğit

doi:10.3390/m649

Abstract

The title compound was prepared by treatment of N,N’-di(4-picolyl¬amino)ethane with N,N-dimethylformamide dimethylacetal in toluene and it was characterized by elemental analysis, 1H NMR and 13C NMR.

Highlights

The title compound was prepared by treatment of N,N’-di(4-picolylamino)ethane with N,N-dimethylformamide dimethylacetal in toluene and it was characterized by elemental analysis, 13 MHz (1H) NMR and 13C NMR
Olefins with four electron-donating substituents react as nucleophiles and are referred to as electron-rich olefins [1,2]
Symmetric electron-rich olefins are generally prepared from an N,N’-disubstituted 1,2-diaminoethane with N,N-dimethylformamide dimethylacetal in an inert atmosphere [11]

Summary

Introduction

Olefins with four electron-donating substituents react as nucleophiles and are referred to as electron-rich olefins [1,2]. Department of Chemistry, Faculty of Science and Art, Adıyaman University, 02040 Adıyaman, Turkey Department of Chemistry, Faculty of Science and Art, InönüUniversity, 44260 Malatya, Turkey 3 Department of Chemistry, Faculty of Science, Ege University, 35100 Bornova-İzmir, Turkey Abstract: The title compound was prepared by treatment of N,N’-di(4-picolylamino)ethane with N,N-dimethylformamide dimethylacetal in toluene and it was characterized by elemental analysis, 1H NMR and 13C NMR.

Results

Conclusion