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Ethyl diazoacetate synthesis in flow

Ethyl diazoacetate is a versatile compound in organic chemistry and frequently used on lab scale. Its highly explosive nature, however, severely limits its use in industrial processes. The in-line coupling of microreactor synthesis and separation technology enables the synthesis of this compound in...

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Autores principales: Delville, Mariëlle M E, van Hest, Jan C M, Rutjes, Floris P J T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778378/
https://www.ncbi.nlm.nih.gov/pubmed/24062847
http://dx.doi.org/10.3762/bjoc.9.211
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author Delville, Mariëlle M E
van Hest, Jan C M
Rutjes, Floris P J T
author_facet Delville, Mariëlle M E
van Hest, Jan C M
Rutjes, Floris P J T
author_sort Delville, Mariëlle M E
collection PubMed
description Ethyl diazoacetate is a versatile compound in organic chemistry and frequently used on lab scale. Its highly explosive nature, however, severely limits its use in industrial processes. The in-line coupling of microreactor synthesis and separation technology enables the synthesis of this compound in an inherently safe manner, thereby making it available on demand in sufficient quantities. Ethyl diazoacetate was prepared in a biphasic mixture comprising an aqueous solution of glycine ethyl ester, sodium nitrite and dichloromethane. Optimization of the reaction was focused on decreasing the residence time with the smallest amount of sodium nitrite possible. With these boundary conditions, a production yield of 20 g EDA day(−1) was achieved using a microreactor with an internal volume of 100 μL. Straightforward scale-up or scale-out of microreactor technology renders this method viable for industrial application.
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spelling pubmed-37783782013-09-23 Ethyl diazoacetate synthesis in flow Delville, Mariëlle M E van Hest, Jan C M Rutjes, Floris P J T Beilstein J Org Chem Full Research Paper Ethyl diazoacetate is a versatile compound in organic chemistry and frequently used on lab scale. Its highly explosive nature, however, severely limits its use in industrial processes. The in-line coupling of microreactor synthesis and separation technology enables the synthesis of this compound in an inherently safe manner, thereby making it available on demand in sufficient quantities. Ethyl diazoacetate was prepared in a biphasic mixture comprising an aqueous solution of glycine ethyl ester, sodium nitrite and dichloromethane. Optimization of the reaction was focused on decreasing the residence time with the smallest amount of sodium nitrite possible. With these boundary conditions, a production yield of 20 g EDA day(−1) was achieved using a microreactor with an internal volume of 100 μL. Straightforward scale-up or scale-out of microreactor technology renders this method viable for industrial application. Beilstein-Institut 2013-09-05 /pmc/articles/PMC3778378/ /pubmed/24062847 http://dx.doi.org/10.3762/bjoc.9.211 Text en Copyright © 2013, Delville et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Delville, Mariëlle M E
van Hest, Jan C M
Rutjes, Floris P J T
Ethyl diazoacetate synthesis in flow
title Ethyl diazoacetate synthesis in flow
title_full Ethyl diazoacetate synthesis in flow
title_fullStr Ethyl diazoacetate synthesis in flow
title_full_unstemmed Ethyl diazoacetate synthesis in flow
title_short Ethyl diazoacetate synthesis in flow
title_sort ethyl diazoacetate synthesis in flow
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3778378/
https://www.ncbi.nlm.nih.gov/pubmed/24062847
http://dx.doi.org/10.3762/bjoc.9.211
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