EventsThe 22nd International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session C. General Organic Synthesis of the event The 22nd International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2018
Citation
Matilde Fondo, Julio Corredoira-Vázquez, Ana María García-Deibe, Jesus Sanmartín-Matalobos, An easy approach to obtain alcohol-amines by reduction of alcohol functionalized imines, in Proceedings of The 22nd International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2018, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-22-05697
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An easy approach to obtain alcohol-amines by reduction of alcohol functionalized imines

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1. Universidad de Santiago de Compostela
Abstract

The reduction of functionalized imines to yield amines is many times an intricate task, since most of the methods described in literature to reduce imines to amines do not take into account that many reducing agents have also basic character. In this way, iminic compounds that have phenol functions usually produce the phenolic salt of the precursor when they are treated with a basic reducing agent, but not the desired amine. In this work, we describe an easy way of isolating very pure aminic compounds with alcoholic functions in its structure from the corresponding iminic compounds, by using NaBH4 as a reducing agent, and avoiding tedious chromatography or multiple solvent extraction steps.

Keywords
Alcohol-amines
alcohol functionalized imines
NaBH4 reducing agent
Manuscript
Poster
J Corredoira Vazquez.pdf
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