Solvent-free organocatalytic preparation of cyclic organic carbonates under scalable continuous flow conditions

2019 ◽  
Vol 4 (1) ◽  
pp. 17-26 ◽  
Author(s):  
Zhiguo Wang ◽  
Romaric Gérardy ◽  
Guillaume Gauron ◽  
Christian Damblon ◽  
Jean-Christophe M. Monbaliu

A solvent-free organocatalyzed process for the transesterification of dimethyl carbonate (DMC) with 1,2-diols under scalable continuous flow conditions.

2020 ◽  
Vol 5 (2) ◽  
pp. 289-299 ◽  
Author(s):  
Abdo-Alslam Alwakwak ◽  
Yingxin He ◽  
Ahmed Almuslem ◽  
Matthew Senter ◽  
Arun K. Itta ◽  
...  

Multifunctional organocatalysts were immobilized on porous hollow fiber polymer and used as intelligent and cooperative heterogeneous catalysts and continuous flow reactor for sustainable chemical transformation.


2019 ◽  
Vol 9 (24) ◽  
pp. 6841-6851 ◽  
Author(s):  
Romaric Gérardy ◽  
Julien Estager ◽  
Patricia Luis ◽  
Damien P. Debecker ◽  
Jean-Christophe M. Monbaliu

A scalable intensified flow process for the preparation of cyclic organic carbonates relying on a cheap ammonium organocatalyst.


2020 ◽  
Vol 22 (8) ◽  
pp. 2359-2364 ◽  
Author(s):  
Patrick Bayer ◽  
Axel Jacobi von Wangelin

Photooxygenations of alkenes with singlet oxygen have been performed under solvent-free conditions in a flow reactor under VIS irradiation. The reaction operates at very high substrate/sensitizer ratios and enables high space–time yields.


2021 ◽  
Vol 50 (7) ◽  
pp. 2493-2500
Author(s):  
Sara Rojas ◽  
Jorge A. R. Navarro ◽  
Patricia Horcajada

A defective Metal-Organic Frameworks as an improved material for the construction of a fixed-bed system working under continuous flow conditions for the removal of the emerging contaminant atenolol.


Tetrahedron ◽  
2021 ◽  
pp. 132305
Author(s):  
Harry R. Smallman ◽  
Jamie A. Leitch ◽  
Tom McBride ◽  
Steven V. Ley ◽  
Duncan L. Browne

Author(s):  
Paolo Zardi ◽  
Michele Maggini ◽  
Tommaso Carofiglio

AbstractThe post-functionalization of porphyrins through the bromination in β position of the pyrrolic rings is a relevant transformation because the resulting bromoderivatives are useful synthons to covalently link a variety of chemical architectures to a porphyrin ring. However, single bromination of porphyrins is a challenging reaction for the abundancy of reactive β-pyrrolic positions in the aromatic macrocycle. We herein report a synthetic procedure for the efficient preparation of 2-bromo-5,10,15,20-tetraphenylporphyrin (1) under continuous flow conditions. The use of flow technology allows to reach an accurate control over critical reaction parameters such as temperature and reaction time. Furthermore, by performing the optimization process through a statistical DoE (Design of Experiment) approach, these parameters could be properly adjusted with a limited number of experiments. This process led us to a better understanding of the relevant factors that govern porphyrins monobromination and to obtain compound 1 with an unprecedent 80% yield.


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