Process Intensification of Tetrazole reaction through tritylation of 5-[4′-(Methyl) Biphenyl-2-Yl] using microreactors
-
Add time:07/13/2019 Source:sciencedirect.com
Currently, process intensification research is focused on use of the continuous micro reactor over the batch reactors. The micro reactor process gives continuous product output, effective micro mixing and better yield in small residence time over batch reactors. A continuous flow process has been successfully developed for the tritylation of 5-(4′-methyl-[1,1′-biphenyl]-2-yl)-1H-tetrazole [MBPT] using different microreactors. The reaction was carried out in three different configurations of microreactors. The SSCR–1 mm and 2 mm (Stainless steel capillary coil micro reactors) gives yield of 93.72 and 92.87% for the residence time of 71 s and 324 s respectively. Among the three microreactors, Corning® AFR afforded effectively higher yield (95.18%) for the residence time of 27 s. Thus, 5-(4′-methyl-[1,1′-biphenyl]-2-yl)-1-trityl-1H-tetrazole, a useful intermediate material for some of the pharmaceutical products that can be produced industrially using microreactor.
We also recommend Trading Suppliers and Manufacturers of 2-(biphenyl-4-yl)-5,6,7,8-tetrahydro-1H-benzo[f]indole (cas 38824-46-3). Pls Click Website Link as below: cas 38824-46-3 suppliers
Prev:Design, synthesis, pharmacological evaluation and computational studies of 1-(biphenyl-4-yl)-2-[4-(substituted phenyl)-piperazin-1-yl]ethanones as potential antipsychotics
Next:Treatment of Takayasu arteritis with the IL-6R antibody tocilizumab vs. cyclophosphamide) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Design, synthesis, pharmacological evaluation and computational studies of 1-(biphenyl-4-yl)-2-[4-(substituted phenyl)-piperazin-1-yl]ethanones as potential antipsychotics07/12/2019
- Theoretical investigation of the vibronic phosphorescence spectra and quantum yields for iridium(III) complexes with 2-(2,5,2′,3′,4′,5′,6′-heptafluoro-biphenyl-4-yl)-pyridine as the primary ligand07/11/2019


