Cargando…

A Protocol for Safe Lithiation Reactions Using Organolithium Reagents

Organolithium reagents are powerful tools in the synthetic chemist's toolbox. However, the extreme pyrophoric nature of the most reactive reagents warrants proper technique, thorough training, and proper personal protective equipment. To aid in the training of researchers using organolithium re...

Descripción completa

Detalles Bibliográficos
Autores principales: Gau, Michael R., Zdilla, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MyJove Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226223/
https://www.ncbi.nlm.nih.gov/pubmed/27911386
http://dx.doi.org/10.3791/54705
_version_ 1782493625990512640
author Gau, Michael R.
Zdilla, Michael J.
author_facet Gau, Michael R.
Zdilla, Michael J.
author_sort Gau, Michael R.
collection PubMed
description Organolithium reagents are powerful tools in the synthetic chemist's toolbox. However, the extreme pyrophoric nature of the most reactive reagents warrants proper technique, thorough training, and proper personal protective equipment. To aid in the training of researchers using organolithium reagents, a thorough, step-by-step protocol for the safe and effective use of tert-butyllithium on an inert gas line or within a glovebox is described. As a model reaction, preparation of lithium tert-butyl amide by the reaction of tert-butyl amine with one equivalent of tert-butyl lithium is presented.
format Online
Article
Text
id pubmed-5226223
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MyJove Corporation
record_format MEDLINE/PubMed
spelling pubmed-52262232017-01-26 A Protocol for Safe Lithiation Reactions Using Organolithium Reagents Gau, Michael R. Zdilla, Michael J. J Vis Exp Chemistry Organolithium reagents are powerful tools in the synthetic chemist's toolbox. However, the extreme pyrophoric nature of the most reactive reagents warrants proper technique, thorough training, and proper personal protective equipment. To aid in the training of researchers using organolithium reagents, a thorough, step-by-step protocol for the safe and effective use of tert-butyllithium on an inert gas line or within a glovebox is described. As a model reaction, preparation of lithium tert-butyl amide by the reaction of tert-butyl amine with one equivalent of tert-butyl lithium is presented. MyJove Corporation 2016-11-12 /pmc/articles/PMC5226223/ /pubmed/27911386 http://dx.doi.org/10.3791/54705 Text en Copyright © 2016, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Chemistry
Gau, Michael R.
Zdilla, Michael J.
A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title_full A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title_fullStr A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title_full_unstemmed A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title_short A Protocol for Safe Lithiation Reactions Using Organolithium Reagents
title_sort protocol for safe lithiation reactions using organolithium reagents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226223/
https://www.ncbi.nlm.nih.gov/pubmed/27911386
http://dx.doi.org/10.3791/54705
work_keys_str_mv AT gaumichaelr aprotocolforsafelithiationreactionsusingorganolithiumreagents
AT zdillamichaelj aprotocolforsafelithiationreactionsusingorganolithiumreagents
AT gaumichaelr protocolforsafelithiationreactionsusingorganolithiumreagents
AT zdillamichaelj protocolforsafelithiationreactionsusingorganolithiumreagents