Synthesis of 2-benzyl N-substituted anilines via imine condensation-isoaromatization of (E)-2-arylidene-3-cyclohexenones and primary amines

Beilstein J Org Chem. 2024 Jul 2:20:1468-1475. doi: 10.3762/bjoc.20.130. eCollection 2024.

Abstract

A catalyst- and additive-free synthesis of 2-benzyl N-substituted anilines from (E)-2-arylidene-3-cyclohexenones and primary amines has been reported. The reaction proceeds smoothly through a sequential imine condensation-isoaromatization pathway, affording a series of synthetically useful aniline derivatives in acceptable to high yields. Mild reaction conditions, no requirement of metal catalysts, operational simplicity and the potential for scale-up production are some of the highlighted advantages of this transformation.

Keywords: (E)-2-arylidene-3-cyclohexenone; aniline; imine condensation; isoaromatization; primary amine.

Grants and funding

This research was founded by the National Natural Science Foundation of China (22161051, 21302163) and Yunnan XingDian Youth Talent Support Program (XDYC-QNRC-2022-0468).