HANNOVER MESSE 2020, 20 - 24 April
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Odorless & requiring almost no cleaning

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Karlsruher Institut für Technologie

Exhibitor details
Exhibitor details
Logo Odorless & requiring almost no cleaning

Product description

Protective groups have important functions in synthetic organic chemistry. Attaching protective groups to a source substance prevents unintended conversion of the functional group in a chemical reaction. In this way, selective conversion can be achieved of one reactive group in the presence of one or more other such groups. Special sulphur protective groups (dithianes or dithiolanes) also offer a possibility to remove the group and, at the same time, introduce other advantageous groupings into the molecule. Synthesizing these dithiane protective groups normally involves organic sulphur compounds which are highly toxic and extremely odorous. Moreover, the individual target substances must be cleaned carefully, which is not only time-consuming but also means extra financial expense caused by the solvents and separating materials required. To overcome these drawbacks, KIT scientists developed a polymer-bound reagent which greatly facilitates the introduction of dithiane protective groups and allows application in parallel synthesis. An aldehyde or ketone as the source material can thus be converted, by means of the reagent and the addition of a solvent, simply, quickly, and safely into the target molecule carrying the protective group. The reagent invented contains two substances needed in protective group synthesis which, because of their polymer binding, are no longer volatile and thus are less toxic and do not smell. In addition, the polymer material inclusive of the reagents and any byproducts generated can be removed from the reaction mix at minimum expense by filtration and evaporation of the solvent.

You can get an overview of this technology at KIT stand. Detailed information can be exchanged individually in contact with the responsible scientific employees of KIT after the industry fair.

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