FlowAct · Flow Chemistry for C-H Activation
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2018-06-01 → 2020-05-31
- EU contribution
- €165,599
- Participants
- 1
- Scheme
- MSCA-IF-EF-ST
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Results in brief
Flow Chemistry for C-H Activation
The general objectives of this project revolved around the recent research field of C-H bond functionalization. Research in this field aims to demonstrate and improve the modification of organic molecules via the activation and subsequent functionalization of C-H bonds, very common in most organic molecules. The abundance of such bonds make them a versatile handle to increase the complexity of organic compounds; moreover, as such modifications do not require pre-functionalized starting materials, they have the advantage, compared to other methods, to considerably reduce the waste generated during the chemical reaction. The reduction of chemical waste has obvious advantages for society, environment, and industry. As C-H bonds are relatively unreactive, specific conditions need to be applied for the process to occur in an effective manner, such as transition metal catalysis, photochemistry, and use of oxidants. Continuous flow chemistry is an alternative methods to perform chemical reactions. In comparison to the classical mixing-and-stirring method typically used, flow chemistry involves pushing the reactants and reagents into a (micro)channel, where the reaction conditions (temperature, pressure, etc) are applied. The advantages of this methods are multiple, including: better heat transfer, better mixing, better irradiation (for photochemical processes), higher safety, and the possibility to continuously monitor the process. In many cases, this results in faster and safer reactions, and better yields and selectivity. Furthermore, it is a continuous method, which makes it suitable for large scale processes. Due to the low reactivity of C-H bonds, and the often low selectivity of their functionalization (due to the many C-H bonds present in a typical molecule), flow chemistry offer the potential to improve the efficiency and applicability of these transformations. The objectives of this project were to demonstrate the efficiency and applicability of continuous flow chemistry techniques to this field. The work undertaken during the action demonstrates that indeed flow chemistry can be effective to improve the outcome of C-H functionalization reactions, with particular effects in reducing the reaction time required, and/or increase the productivity in a continuous process. Good part of this work for carried out for light promoted transformations, which offer even more waste-reducing alternatives than metal-catalysed reactions, and for which flow chemistry shows even better performances.
Data: CORDIS, © European Union
Project objective
The metal-catalysed group-directed functionalisation of C-H bonds is emerging as an important synthetic methodology in organic chemistry. Despite the advances in the field, however, C-H functionalisation processes are still plagued by several disadvantages, such as selectivity and reproducibility issues, the necessity of directing-group (DG) introduction, and the often difficult DG cleavage. This proposal combines the development of novel chemical transformations with the use of flow microreactors to: 1)make the DG introduction and cleavage more efficient and synthetically useful, and 2) make the C-H functionalisation processes more selective and atom economic, thus addressing several important weaknesses of this type of chemistry. After the development of the individual transformations in continuous-flow, the three crucial steps (DG introduction, group-directed C-H functionalisation and DG cleavage) will be integrated in a combined, multistep protocol, with the aim of minimising purification steps, and ultimately provide a cleaner and faster synthesis of functionalised molecules in a single continuous process.
Original text from CORDIS.
Participants
- TECHNISCHE UNIVERSITEIT EINDHOVEN · EindhovenCoordinatorNetherlands
Links
Data: CORDIS, © European Union
