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Mechanochemical Knoevenagel condensation investigated in situ

The mechanochemical Knoevenagel condensation of malononitrile with p-nitrobenzaldehyde was studied in situ using a tandem approach. X-ray diffraction and Raman spectroscopy were combined to yield time-resolved information on the milling process. Under solvent-free conditions, the reaction leads to a...

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Autores principales: Haferkamp, Sebastian, Fischer, Franziska, Kraus, Werner, Emmerling, Franziska
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629385/
https://www.ncbi.nlm.nih.gov/pubmed/29062421
http://dx.doi.org/10.3762/bjoc.13.197
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author Haferkamp, Sebastian
Fischer, Franziska
Kraus, Werner
Emmerling, Franziska
author_facet Haferkamp, Sebastian
Fischer, Franziska
Kraus, Werner
Emmerling, Franziska
author_sort Haferkamp, Sebastian
collection PubMed
description The mechanochemical Knoevenagel condensation of malononitrile with p-nitrobenzaldehyde was studied in situ using a tandem approach. X-ray diffraction and Raman spectroscopy were combined to yield time-resolved information on the milling process. Under solvent-free conditions, the reaction leads to a quantitative conversion to p-nitrobenzylidenemalononitrile within 50 minutes. The in situ data indicate that the process is fast and proceeds under a direct conversion. After stopping the milling process, the reaction continues until complete conversion. The continuous and the stopped milling process both result in crystalline products suitable for single crystal X-ray diffraction.
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spelling pubmed-56293852017-10-23 Mechanochemical Knoevenagel condensation investigated in situ Haferkamp, Sebastian Fischer, Franziska Kraus, Werner Emmerling, Franziska Beilstein J Org Chem Full Research Paper The mechanochemical Knoevenagel condensation of malononitrile with p-nitrobenzaldehyde was studied in situ using a tandem approach. X-ray diffraction and Raman spectroscopy were combined to yield time-resolved information on the milling process. Under solvent-free conditions, the reaction leads to a quantitative conversion to p-nitrobenzylidenemalononitrile within 50 minutes. The in situ data indicate that the process is fast and proceeds under a direct conversion. After stopping the milling process, the reaction continues until complete conversion. The continuous and the stopped milling process both result in crystalline products suitable for single crystal X-ray diffraction. Beilstein-Institut 2017-09-26 /pmc/articles/PMC5629385/ /pubmed/29062421 http://dx.doi.org/10.3762/bjoc.13.197 Text en Copyright © 2017, Haferkamp et al. https://creativecommons.org/licenses/by/4.0https://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/4.0), 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
Haferkamp, Sebastian
Fischer, Franziska
Kraus, Werner
Emmerling, Franziska
Mechanochemical Knoevenagel condensation investigated in situ
title Mechanochemical Knoevenagel condensation investigated in situ
title_full Mechanochemical Knoevenagel condensation investigated in situ
title_fullStr Mechanochemical Knoevenagel condensation investigated in situ
title_full_unstemmed Mechanochemical Knoevenagel condensation investigated in situ
title_short Mechanochemical Knoevenagel condensation investigated in situ
title_sort mechanochemical knoevenagel condensation investigated in situ
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5629385/
https://www.ncbi.nlm.nih.gov/pubmed/29062421
http://dx.doi.org/10.3762/bjoc.13.197
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AT emmerlingfranziska mechanochemicalknoevenagelcondensationinvestigatedinsitu