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An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)

1,1,6-Trimethyl-1,2-dihydronaphthalene (TDN), an aroma compound present in wine, is used for sensory and physicochemical analyses. Therefore, synthesis of TDN of high purity is required for these purposes. Optimization of TDN synthesis in order to facilitate its subsequent purification was described...

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Detalles Bibliográficos
Autores principales: Dobrydnev, Alexey, Tarasov, Andrii, Müller, Nikolaus, Volovenko, Yulian, Rauhut, Doris, Jung, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938800/
https://www.ncbi.nlm.nih.gov/pubmed/31908985
http://dx.doi.org/10.1016/j.mex.2019.12.009
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author Dobrydnev, Alexey
Tarasov, Andrii
Müller, Nikolaus
Volovenko, Yulian
Rauhut, Doris
Jung, Rainer
author_facet Dobrydnev, Alexey
Tarasov, Andrii
Müller, Nikolaus
Volovenko, Yulian
Rauhut, Doris
Jung, Rainer
author_sort Dobrydnev, Alexey
collection PubMed
description 1,1,6-Trimethyl-1,2-dihydronaphthalene (TDN), an aroma compound present in wine, is used for sensory and physicochemical analyses. Therefore, synthesis of TDN of high purity is required for these purposes. Optimization of TDN synthesis in order to facilitate its subsequent purification was described. As a result, ≥99.5 % of TDN purity was reached. • The possibility of using both α-ionone and β-ionone as starting substances was demonstrated; • Modifications of the use of reagents in the second and third steps of TDN synthesis were proposed.
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spelling pubmed-69388002020-01-06 An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN) Dobrydnev, Alexey Tarasov, Andrii Müller, Nikolaus Volovenko, Yulian Rauhut, Doris Jung, Rainer MethodsX Chemistry 1,1,6-Trimethyl-1,2-dihydronaphthalene (TDN), an aroma compound present in wine, is used for sensory and physicochemical analyses. Therefore, synthesis of TDN of high purity is required for these purposes. Optimization of TDN synthesis in order to facilitate its subsequent purification was described. As a result, ≥99.5 % of TDN purity was reached. • The possibility of using both α-ionone and β-ionone as starting substances was demonstrated; • Modifications of the use of reagents in the second and third steps of TDN synthesis were proposed. Elsevier 2019-12-16 /pmc/articles/PMC6938800/ /pubmed/31908985 http://dx.doi.org/10.1016/j.mex.2019.12.009 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Chemistry
Dobrydnev, Alexey
Tarasov, Andrii
Müller, Nikolaus
Volovenko, Yulian
Rauhut, Doris
Jung, Rainer
An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title_full An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title_fullStr An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title_full_unstemmed An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title_short An optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (TDN)
title_sort optimized method for synthesis and purification of 1,1,6-trimethyl-1,2-dihydronaphthalene (tdn)
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938800/
https://www.ncbi.nlm.nih.gov/pubmed/31908985
http://dx.doi.org/10.1016/j.mex.2019.12.009
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