News Release

Creating complex molecules in just a few steps


Peer-Reviewed Publication

Ruhr-University Bochum

Stefania Trita and Lukas Gooßen, Ruhr-University Bochum

image: Lukas Gooßen and Stefania Trita are working on procedures that are supposed to make the production of chemical substances cheaper and more environmentally friendly. view more 

Credit: RUB, Marquard

The team of the Ruhr-Universität Bochum around Prof Dr Lukas Gooßen and Stefania Trita describe the process together with a colleague of the University of Kaiserslautern in the journal Angewandte Chemie.

"Existing industrial processes for the synthesis of complex molecules often have the disadvantage that they require many steps and that a lot of waste is generated, especially salts," says Lukas Gooßen, Evonik Chair of Organic Chemistry I and member of the Cluster of Excellence Resolv. One solution may be C-H activation.

Was considered impossible

Bonds between carbon (C) and hydrogen (H) are the most common chemical bonds, both in nature and in artificial chemicals. They are very stable and are reluctant to undergo chemical reactions. "For that reason, it had long been considered impossible to transform these bonds into functional groups that are essential, for example, for drug efficacy," Gooßen explains.

The biggest challenge is to transform one particular C-H bond in one molecule whilst leaving the others untouched. In the current study the scientists worked with benzoic acids, which consist of a carbon ring and an acid group. With the new method they specifically converted a single C-H bond on the carbon ring into a C-C bond. This enabled them to easily combine two different molecules to form a more complex product.

Low temperature, less waste

"One advantage is that we need a low reaction temperature of only 50 degrees Celsius and that no waste products are created," Gooßen summarises. "We hope that one day the process will enable complex pharmaceutical chemicals and substances required in agriculture to be produced in fewer steps than before and in a more energy-efficient, environmentally friendly and cost-effective manner."

The choice of solvent was crucial for an efficient reaction. "With commercially available solvents, we initially achieved a very low yield of the desired product," says Lukas Gooßen. With trichloroethanol, the yield was significantly increased.



The work was funded by the Deutsche Forschungsgemeinschaft (German Research Foundation) as part of the Cluster of Excellence Resolv (EXC 1069) and the Collaborative Research Centre SFB/TRR 88 and also by the Alexander-von-Humboldt Stiftung (Scholarship to author Martin Pichette-Drapeau).

Original publication

Stefania Trita, Agostino Biafora, Martin Pichette-Drapeau, Philip Weber, Lukas J. Goossen: Regiospecific ortho-C-H Allylation of Benzoic Acids, in: Angewandte Chemie International Edition, 2018, DOI: 10.1002/anie.201712520,

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