Issue 39, 2014

Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides

Abstract

Ultrasound-assisted solventless oxidation/reductive amination of benzyl halides was developed as a facile, efficient, and environmental friendly method toward N-alkylated amines. Aldehydes were formed in situ by oxidation of organic halides with N-methylmorpholine N-oxide (NMO), followed by direct reductive amination with amines using sodium borohydride and montmorillonite K-10 catalyst as the reducing system. This green and simple procedure enables N-alkylated amines to be prepared in good to excellent yields with high selectivity of the monoalkylation.

Graphical abstract: Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides

Supplementary files

Article information

Article type
Communication
Submitted
03 Apr 2014
Accepted
25 Apr 2014
First published
08 May 2014

RSC Adv., 2014,4, 20454-20458

Author version available

Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides

B. Khumraksa, W. Phakhodee and M. Pattarawarapan, RSC Adv., 2014, 4, 20454 DOI: 10.1039/C4RA02969K

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