Five-membered cyclic sulfamidates are very valuable electrophiles in organic synthesis and readily used on a multikilogram scale. However, their thermal degradation is underreported and might lead to unforeseen and undesirable safety events. In addition, ring or nitrogen substitution can have a tremendous influence on cyclic sulfamidate reactivity toward bases and therefore impact the overall safety assessment of a process. An understanding of such behavior is therefore of high importance in the industry while designing a synthetic route, as a change of, e.g., a protecting group can increase the thermal safety of a step on scale. We report herein the thermal degradation investigation as well as the structure-related reactivity exploration of cyclic sulfamidates, including their use in combination with strong bases. The design of a predictive model to rapidly assess the thermal hazard based on collected data and selected molecular descriptors is also presented.
Before scaling up to production, it is of high importance to evaluate the potential of a reaction to lead to an undesired thermal degradation event. The use of a large amount of compounds is usually required for a reliable calorimetry study. In this work, we report the development of a milliliter-scale reaction calorimeter for reaction screening applications. The setup was designed using laboratory equipment and characterized and validated with routine experiments. The results were sufficiently accurate enabling us to observe trends in the measured reaction enthalpies of a family of compounds reacting with strong bases as a function of the compounds' structures.. The use of the microscale tailor-made calorimeter is considered very valuable for potentially highly energetic reactions since reaction calorimetry studies can be performed accurately and safely with small amounts of valuable materials.
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