scholarly journals Greener Synthesis of Pristane by Flow Dehydrative Hydrogenation of Allylic Alcohol Using a Packed-Bed Reactor Charged by Pd/C as a Single Catalyst

Molecules ◽  
2021 ◽  
Vol 26 (19) ◽  
pp. 5845
Author(s):  
Takayoshi Kasakado ◽  
Yuki Hirobe ◽  
Akihiro Furuta ◽  
Mamoru Hyodo ◽  
Takahide Fukuyama ◽  
...  

Our previous work established a continuous-flow synthesis of pristane, which is a saturated branched alkane obtained from a Basking Shark. The dehydration of an allylic alcohol that is the key to a tetraene was carried out using a packed-bed reactor charged by an acid–silica catalyst (HO-SAS) and flow hydrogenation using molecular hydrogen via a Pd/C catalyst followed. The present work relies on the additional propensity of Pd/C to serve as an acid catalyst, which allows us to perform a flow synthesis of pristane from the aforementioned key allylic alcohol in the presence of molecular hydrogen using Pd/C as a single catalyst, which is applied to both dehydration and hydrogenation. The present one-column-two-reaction-flow system could eliminate the use of an acid catalyst such as HO-SAS and lead to a significant simplification of the production process.

2012 ◽  
Vol 79 ◽  
pp. 1-7 ◽  
Author(s):  
A.V.P. Albertini ◽  
A.L.S. Reis ◽  
F.R.R. Teles ◽  
J.C. Souza ◽  
J.L. Rolim Filho ◽  
...  

2020 ◽  
Vol 22 (21) ◽  
pp. 7398-7405 ◽  
Author(s):  
Jose Alirio Mendoza Mesa ◽  
Francesco Brandi ◽  
Irina Shekova ◽  
Markus Antonietti ◽  
Majd Al-Naji

The continuous flow synthesis of p-xylene (pXL) via Diels–Alder cycloaddition of lignocellulosic biomass-derivable 2,5-dimethylfuran (DMF) and acrylic acid (AA) was performed over different types of zeolites.


2018 ◽  
Vol 54 (7) ◽  
pp. 825-828 ◽  
Author(s):  
M. B. Johansen ◽  
A. T. Lindhardt

A simple to prepare, dry and handle packed bed reactor carrying CsF on CaF2, towards nucleophilic fluorinations in continuous flow, is reported.


2018 ◽  
Vol 38 (2) ◽  
pp. 270-276 ◽  
Author(s):  
Izabela R. C. Araujo ◽  
Simone D. Gomes ◽  
Tamiris U. Tonello ◽  
Shaiane Dal'Maso Lucas ◽  
Angelo G. Mari ◽  
...  

2017 ◽  
Vol 13 ◽  
pp. 239-246 ◽  
Author(s):  
Ananda Herath ◽  
Nicholas D P Cosford

A versatile continuous-flow synthesis of highly functionalized 1,2,4-oxadiazoles starting from carboxylic acids is reported. This process was applied to the multistep synthesis of imidazo[1,2-a]pyridin-2-yl-1,2,4-oxadiazoles, using a three reactor, multistep continuous-flow system without isolation of intermediates. This continuous-flow method was successfully combined with a single-step liquid–liquid microextraction unit to remove high boiling point polar solvents and impurities and provides the target compounds in high purity with excellent overall yields.


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