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Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand
A convenient three-step preparation of the dinucleating ligand, 1,6-bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane (3) starting from 2,6-bis(hydroxymethyl)-4-methylphenol (4) is reported. Compound 4 was partially oxidized with preactivated manganese dioxide to form compound...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236381/ http://dx.doi.org/10.3390/61201001 |
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author | Sun, Gang-Chun He, Zhan-Hang Li, Zhong-Jun Yuan, Xiao-Dong Yang, Zhi-Juan Wang, Guo-Xi Wang, Liu-Fang Liu, Chang-Rang |
author_facet | Sun, Gang-Chun He, Zhan-Hang Li, Zhong-Jun Yuan, Xiao-Dong Yang, Zhi-Juan Wang, Guo-Xi Wang, Liu-Fang Liu, Chang-Rang |
author_sort | Sun, Gang-Chun |
collection | PubMed |
description | A convenient three-step preparation of the dinucleating ligand, 1,6-bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane (3) starting from 2,6-bis(hydroxymethyl)-4-methylphenol (4) is reported. Compound 4 was partially oxidized with preactivated manganese dioxide to form compound 5, which was converted to 2-hydroxy-3-chloromethyl-5-ethylbenzaldehyde (6) with conc.HCl/EtOH. Compound 6 in turn reacted with N,N’-bis (2-furyl)-1,2-diaminoethane (7) in the presence of K(2)CO(3) in ethanol to give the title compound 3. No protecting groups were required in the whole process and the conditions were mild. |
format | Online Article Text |
id | pubmed-6236381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62363812018-11-20 Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand Sun, Gang-Chun He, Zhan-Hang Li, Zhong-Jun Yuan, Xiao-Dong Yang, Zhi-Juan Wang, Guo-Xi Wang, Liu-Fang Liu, Chang-Rang Molecules Article A convenient three-step preparation of the dinucleating ligand, 1,6-bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane (3) starting from 2,6-bis(hydroxymethyl)-4-methylphenol (4) is reported. Compound 4 was partially oxidized with preactivated manganese dioxide to form compound 5, which was converted to 2-hydroxy-3-chloromethyl-5-ethylbenzaldehyde (6) with conc.HCl/EtOH. Compound 6 in turn reacted with N,N’-bis (2-furyl)-1,2-diaminoethane (7) in the presence of K(2)CO(3) in ethanol to give the title compound 3. No protecting groups were required in the whole process and the conditions were mild. MDPI 2001-11-30 /pmc/articles/PMC6236381/ http://dx.doi.org/10.3390/61201001 Text en © 2001 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Article Sun, Gang-Chun He, Zhan-Hang Li, Zhong-Jun Yuan, Xiao-Dong Yang, Zhi-Juan Wang, Guo-Xi Wang, Liu-Fang Liu, Chang-Rang Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title | Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title_full | Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title_fullStr | Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title_full_unstemmed | Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title_short | Facile Synthesis of 1,6-Bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a New Dinucleating Ligand |
title_sort | facile synthesis of 1,6-bis(2-furyl)-2,5-bis(2-hydroxy-3-formyl-5-methylbenzyl)-2,5-diazahexane: a new dinucleating ligand |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236381/ http://dx.doi.org/10.3390/61201001 |
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