Transition Metal-free Methylation of Amines with Formaldehyde as the Reductant and Methyl Source
Author(s) -
Nikki Y. T. Man,
Wanfang Li,
Scott G. Stewart,
XiaoFeng Wu
Publication year - 2015
Publication title -
chimia international journal for chemistry
Language(s) - English
Resource type - Journals
eISSN - 2673-2424
pISSN - 0009-4293
DOI - 10.2533/chimia.2015.345
Subject(s) - formaldehyde , steric effects , chemistry , methylation , transition metal , primary (astronomy) , metal , organic chemistry , catalysis , biochemistry , physics , astronomy , gene
A simple transition metal-free procedure using formal dehyde for the N,N-dimethylation and N-methylation of primary and secondary anilines is reported. The reaction showed limitations on sterically hindered and electron-withdrawing anilines, but is successful on amines with electron-donating substituents. Formaldehyde acts as both the reducing agent and the carbon source in the reaction.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom