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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Online Access: | https://doi.org/10.3762/bjoc.9.211 |
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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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1724308442027393024 |