Synthesis 2020; 52(02): 281-289
DOI: 10.1055/s-0039-1690731
paper
© Georg Thieme Verlag Stuttgart · New York

Efficient Synthesis of Diarylmethylamines via Lewis Acid Catalyzed Friedel–Crafts Reactions of Donor–Acceptor Aziridines with N,N-Dialkylanilines

Yerin Kim
,
Yong Il Kwon
,
Sung-Gon Kim
Department of Chemistry, Kyonggi University, 154-42 Gwanggyosan-ro, Yeongtong-gu, Suwon 16227, Republic of Korea   eMail: sgkim123@kyonggi.ac.kr
› Institutsangaben

This research was supported by the Nanomaterial Technology Development Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (NRF-2012M3A7B4049645) and the Basic Science Research Program through NRF funded by the Ministry of Education (NRF-2016R1D1A1A09916621), and by Kyonggi University's Graduate Research Assistant Fellowship 2019.
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Publikationsverlauf

Received: 02. August 2019

Accepted after revision: 08. Oktober 2019

Publikationsdatum:
29. Oktober 2019 (online)


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Abstract

A method for efficient and mild synthesis of diarylmethylamine scaffold, via Lewis acid catalyzed Friedel–Crafts reaction of donor­–acceptor aziridines with N,N-dialkylanilines to afford a biologically important diarylmethylamine derivatives in high yields (up to 88%), is presented. This reaction is suitable for the synthesis of various diarylmethylamine derivatives and has a broad scope for electron-rich arenes, including dimethoxybenzene.

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