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

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 r...

Full description

Saved in:
Bibliographic Details
Main Authors: Bannarak Khumraksa, Wong Phakhodee, Mookda Pattarawarapan
Format: Journal
Published: 2018
Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901257342&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45299
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Chiang Mai University
id th-cmuir.6653943832-45299
record_format dspace
spelling th-cmuir.6653943832-452992018-01-24T06:08:06Z Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides Bannarak Khumraksa Wong Phakhodee Mookda Pattarawarapan 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. This journal is © the Partner Organisations 2014. 2018-01-24T06:08:06Z 2018-01-24T06:08:06Z 2014-01-01 Journal 20462069 2-s2.0-84901257342 10.1039/c4ra02969k https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901257342&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/45299
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
description 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. This journal is © the Partner Organisations 2014.
format Journal
author Bannarak Khumraksa
Wong Phakhodee
Mookda Pattarawarapan
spellingShingle Bannarak Khumraksa
Wong Phakhodee
Mookda Pattarawarapan
Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
author_facet Bannarak Khumraksa
Wong Phakhodee
Mookda Pattarawarapan
author_sort Bannarak Khumraksa
title Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
title_short Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
title_full Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
title_fullStr Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
title_full_unstemmed Ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
title_sort ultrasound-assisted solventless synthesis of amines by in situ oxidation/reductive amination of benzyl halides
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84901257342&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/45299
_version_ 1681422719385600000