Abstract
On-flow ReactIR and 1H NMR reaction monitoring, coupled with in situ intermediate characterization, was used to aid in the mechanistic elucidation of the N-chlorosuccinimide mediated transformation of an α-thioamide. Multiple intermediates in this reaction cascade are identified and characterized, and in particular, spectroscopic evidence for the intermediacy of the chlorosulfonium ion in the chlorination of α-thioamides is provided. Further to this, solvent effects on the outcome of the transformation are discussed. This work also demonstrates the utility of using a combination of ReactIR and flow NMR reaction monitoring (ReactNMR) for characterizing complex multicomponent reaction mixtures.
| Original language | English |
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| Pages (from-to) | 9630-9640 |
| Number of pages | 11 |
| Journal | Journal of Organic Chemistry |
| Volume | 76 |
| Issue number | 23 |
| DOIs | |
| Publication status | Published - 2 Dec 2011 |