Gram‐Scale Synthesis of the 1,1, n , n ‐Tetramethyl[ n ](2,11)teropyrenophanes
Autor: | Kiran Sagar Unikela, Parisa Ghods Ghasemabadi, Graham J. Bodwell, Yuming Zhao, Louise N. Dawe, Václav Houska |
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Rok vydání: | 2020 |
Předmět: | |
Zdroj: | Chemistry – A European Journal. 27:390-400 |
ISSN: | 1521-3765 0947-6539 |
Popis: | A gram-scale synthesis of a series of 1,1,n,n-tetramethyl[n](2,11)teropyrenophanes (n=7-9) has been accomplished as well as the first synthesis of the next higher homologue 1,1,10,10-tetramethyl[10](2,11)teropyrenophane. The scale-up of the original small-scale synthesis required the development of several heavily modified synthetic methods, including a chlorination/Friedel-Crafts alkylation protocol and an iodination/Wurtz coupling protocol, which were performed on 25-30 g and 30-60 g scales, respectively. Two separate sets of conditions for the key teropyrene-forming cyclodehydrogenation reaction at the end of the synthetic pathway were developed, an acid-promoted one for the two less strained congeners and an acid-free method for the two more strained homologues. |
Databáze: | OpenAIRE |
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