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Abstract In synthetic method development, the most rewarding path is seldom a straight line. While our initial entry into pentafluorosulfanyl (SF 5 ) chemistry did not go according to plan (due to inaccessibility of reagents such as SF 5 Cl at the time), a “detour” led us to establish mild and inexpensive oxidative fluorination conditions that made aryl‐SF 5 compound synthesis more accessible. The method involved the use of potassium fluoride and trichloroisocyanuric acid (TCICA)—a common swimming pool disinfectant—as opposed to previously employed reagents such as F 2 , XeF 2 , HF, and Cl 2 . Thereafter, curiosity led us to explore applications of TCICA/KF as a more general approach to the synthesis of fluorinated Group 15, 16, and 17 heteroatoms in organic scaffolds; this, in turn, prompted SC‐XRD, VT‐NMR, computational, and physical organic studies. Ultimately, it was discovered that TCICA/KF can be used to synthesize SF 5 Cl, enabling SF 5 chemistry in an unexpected way.
Kraemer et al. (Tue,) studied this question.