Abstract
A three-component coupling reaction of phenylacetylene, p-toluenesulfonyl azide, and water through copper catalysis is described to provide knowledge of spectroscopy and catalytic reactions and to introduce current research topics in organic chemistry for second-year undergraduate students. In the presence of stoichiometric amounts of phenylacetylene, p-toluenesulfonyl azide, and triethylamine, the reaction was performed with 4 mol% CuCl in water as the sole solvent and was completed in 1.5 h. A practical purification method and recrystallization of the crude reaction mixture resulted in the rapid isolation of the desired product with yields of 42~65%. Students characterized 4-methyl-N-(phenylacetyl)benzenesulfonamide by using melting-point determination, infrared spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. This experimental procedure and spectroscopic data analysis will serve as a platform for students to apply classroom knowledge in practical state-of-the-art research.
Original language | English |
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Pages (from-to) | 187-190 |
Number of pages | 4 |
Journal | Journal of the Korean Chemical Society |
Volume | 62 |
Issue number | 3 |
DOIs | |
State | Published - 2018 |
Bibliographical note
Publisher Copyright:© Korean Chemical Society. All Rights Reserved.
Keywords
- Alkynes
- Amides
- Catalysis
- Inquiry-based/discovery learning
- Spectroscopy