Novel 1,2,3-Triazole-Bisphenol-Based Macrocycle Synthesized Through Click Chemistry

Title:Novel 1,2,3-Triazole-Bisphenol-Based Macrocycle Synthesized Through Click Chemistry

Volume: 10 Issue: 10

Author(s): Burhan Khan, Said Nadeem, Muhammad R. Shah, Sammer Yousuf and Numan Hoda

Affiliation:

Keywords: Bisphenol, click chemistry, 1, 3-dipolar cycloadditions, macrocycles, 1, 2, 3-triazole.

Abstract: A flexible macrocycle 7 based on 1,2,3-triazole and biphenol was synthesized through click chemistry and it contained propyl group. Click chemistry was used to get macrocycle 7 by reacting diazide 4 and diyne 6 in the presence of ascorbic acid. EI-MS of macrocycle 7 showed molecular ion peak at 614.3 while ESI-MS showed 615.25 [M+H]⁺. ¹H NMR of 7 showed the proton of propyl -CH₂- at 2.26, 3.81 and 4.56 ppm while a singlet was observed at 5.26 ppm whi ch belonged to methylene protons located between triazole ring and phenol. The aromatic proton at triazole ring was observed at 8.17 ppm while the protons of biphenyl were observed between 6.42 and 7.50 ppm. Crystallographic data of 3 were submitted to CCDC library (893412).

Cite this article as:

Khan Burhan, Nadeem Said, Shah R. Muhammad, Yousuf Sammer and Hoda Numan, Novel 1,2,3-Triazole-Bisphenol-Based Macrocycle Synthesized Through Click Chemistry, Letters in Organic Chemistry 2013; 10 (10) . https://dx.doi.org/10.2174/15701786113109990040