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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Main Authors: Mariëlle M. E. Delville, Jan C. M. van Hest, Floris P. J. T. Rutjes
Format: Article
Language:English
Published: Beilstein-Institut 2013-09-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.9.211
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spelling doaj-effa7524c16246c9888c29f3872d91d12021-02-02T03:13:06ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972013-09-01911813181810.3762/bjoc.9.2111860-5397-9-211Ethyl diazoacetate synthesis in flowMariëlle M. E. Delville0Jan C. M. van Hest1Floris P. J. T. Rutjes2Radboud University Nijmegen, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, the NetherlandsRadboud University Nijmegen, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, the NetherlandsRadboud University Nijmegen, Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen, the NetherlandsEthyl 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.https://doi.org/10.3762/bjoc.9.211diazo compoundsdiazotizationethyl diazoacetate (EDA)flow chemistrymicroreactor technology
collection DOAJ
language English
format Article
sources DOAJ
author Mariëlle M. E. Delville
Jan C. M. van Hest
Floris P. J. T. Rutjes
spellingShingle Mariëlle M. E. Delville
Jan C. M. van Hest
Floris P. J. T. Rutjes
Ethyl diazoacetate synthesis in flow
Beilstein Journal of Organic Chemistry
diazo compounds
diazotization
ethyl diazoacetate (EDA)
flow chemistry
microreactor technology
author_facet Mariëlle M. E. Delville
Jan C. M. van Hest
Floris P. J. T. Rutjes
author_sort Mariëlle M. E. Delville
title Ethyl diazoacetate synthesis in flow
title_short 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_sort ethyl diazoacetate synthesis in flow
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2013-09-01
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.
topic diazo compounds
diazotization
ethyl diazoacetate (EDA)
flow chemistry
microreactor technology
url https://doi.org/10.3762/bjoc.9.211
work_keys_str_mv AT mariellemedelville ethyldiazoacetatesynthesisinflow
AT jancmvanhest ethyldiazoacetatesynthesisinflow
AT florispjtrutjes ethyldiazoacetatesynthesisinflow
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