Abstract
Chemists often use an amine group as an intermediate in syntheses of imines, amides and ureas; however, in the case of syntheses of p-aminophenol type compounds, several problems might occur. In this article, we prepared p-aminocalix[5]arene-pentaol by reduction of both nitro and azo derivatives, and compared four methods of the amine preparation, focusing mainly on its gramme scale and time-consuming issues.
Original language | English |
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Pages (from-to) | 450-454 |
Number of pages | 5 |
Journal | Supramolecular Chemistry |
Volume | 28 |
Issue number | 5-6 |
Early online date | 11 Dec 2015 |
DOIs | |
Publication status | Published - 2 Jun 2016 |
Keywords
- amine
- azo coupling
- Calixarene
- nitration