Table salt as a catalyst for the oxidation of aromatic alcohols and amines to acids and imines in aqueous medium: effectively carrying out oxidation reactions in sea water

2019 ◽  
Vol 21 (8) ◽  
pp. 1929-1934 ◽  
Author(s):  
Susanta Hazra ◽  
Ajay Kishor Kushawaha ◽  
Deepak Yadav ◽  
Pritam Dolui ◽  
Mayukh Deb ◽  
...  

A simple, efficient, sustainable and economical method for the oxidation of alcohols and amines has been developed using chloride, a sea abundant anionic catalyst for the synthesis of a range of carboxylic acids, ketones and imines.

2018 ◽  
Vol 20 (13) ◽  
pp. 3038-3043 ◽  
Author(s):  
Kai-Jian Liu ◽  
Si Jiang ◽  
Ling-Hui Lu ◽  
Ling-Li Tang ◽  
Shan-Shan Tang ◽  
...  

A practical and eco-friendly protocol for the oxidation of alcohols into carboxylic acids and ketones under metal-, base- and additive-free conditions is reported.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Fatemeh Azimi ◽  
Ahmad Poursattar Marjani ◽  
Sajjad Keshipour

AbstractManipulation of materials is considered as one of the eminent strategies to create desirable catalysts. In this regard, increasing surface area and decreasing dimensions of catalysts have been widely employed on account of effectiveness of these methods. Herein, aerogel form of chitosan as a sustainable, and high aspect ratio compound is employed as a green support for the catalytic purposes. Chitosan aerogel was modified with Fe(II)-phthalocyanine to produce a heterogeneous catalyst for oxidation reactions. The synthesized catalyst promoted the oxidation reactions of alcohols and alkyl arenes to the corresponding aldehydes and ketones using H2O2 as an oxidant in 24 h. The reactions for aliphatic and aromatic alcohols gave turnover numbers of 106–109 at 80 °C and 106–117 at room temperature, respectively. The oxidations of alkyl arenes were carried out with turnover numbers laying in the range of 106–117 at 100 °C. The low toxicity, inexpensive nature, and recycling possibility of the catalyst accompanied by the reaction mild conditions, clean oxidant, and excellent yields offer chitosan aerogel modified with Fe(II)-phthalocyanine as a promising catalyst for oxidation reactions.


Molecules ◽  
2020 ◽  
Vol 25 (2) ◽  
pp. 364 ◽  
Author(s):  
Kendra Leahy Denlinger ◽  
Preston Carr ◽  
Daniel C. Waddell ◽  
James Mack

The oxidation of primary alcohols under mechanochemical conditions in a Spex8000M Mixer/Mill was investigated. To facilitate ease of separation and recyclability, a polystyrene-bound version of a TEMPO catalyst was employed. When paired with Oxone® in a stainless-steel vial with a stainless-steel ball, several primary alcohols were successfully oxidized to the corresponding carboxylic acids. The product was isolated using gravity filtration, which also allowed for the polystyrene-bound TEMPO catalyst to be recovered and reused in subsequent oxidation reactions. Furthermore, it was demonstrated that the size and steric hindrance of the primary alcohol does not hinder the rate of the reaction. Finally, the aldehyde was selectively obtained from a primary alcohol under ball milling conditions by using a combination of non-supported TEMPO with a copper vial and copper ball.


2021 ◽  
Vol 22 (13) ◽  
pp. 6787
Author(s):  
Constantin I. Tănase ◽  
Constantin Drăghici ◽  
Miron Teodor Căproiu ◽  
Anamaria Hanganu ◽  
Gheorghe Borodi ◽  
...  

β-Ketophosphonates with pentalenofurane fragments linked to the keto group were synthesized. The bulky pentalenofurane skeleton is expected to introduce more hindrance in the prostaglandin analogues of type III, greater than that obtained with the bicyclo[3.3.0]oct(a)ene fragments of prostaglandin analogues I and II, to slow down (retard) the inactivation of the prostaglandin analogues by oxidation of 15α-OH to the 15-keto group via the 15-PGDH pathway. Their synthesis was performed by a sequence of three high yield reactions, starting from the pentalenofurane alcohols 2, oxidation of alcohols to acids 3, esterification of acids 3 to methyl esters 4 and reaction of the esters 4 with lithium salt of dimethyl methanephosphonate at low temperature. The secondary compounds 6b and 6c were formed in small amounts in the oxidation reactions of 2b and 2c, and the NMR spectroscopy showed that their structure is that of an ester of the acid with the starting alcohol. Their molecular structures were confirmed by single crystal X-ray determination method for 6c and XRPD powder method for 6b.


2015 ◽  
Vol 14 (3) ◽  
pp. 563-568 ◽  
Author(s):  
Theodoros S. Symeonidis ◽  
Ioannis Tamiolakis ◽  
Gerasimos S. Armatas ◽  
Ioannis N. Lykakis

Decatungstate supported on mesoporous TiO2 nanoparticle assemblies catalyze the selective and efficient oxidation of aromatic alcohols under “green” oxidation conditions. An electron transfer mechanism was predominated under UV-vis irradiation.


ACS Catalysis ◽  
2018 ◽  
Vol 8 (7) ◽  
pp. 6738-6744 ◽  
Author(s):  
Mohammad Rafiee ◽  
Zachary M. Konz ◽  
Matthew D. Graaf ◽  
Hannes F. Koolman ◽  
Shannon S. Stahl

2018 ◽  
Vol 32 (12) ◽  
pp. e4574 ◽  
Author(s):  
Ajeet Singh ◽  
Sandip K. Singh ◽  
Anoop K. Saini ◽  
Shaikh M. Mobin ◽  
Pradeep Mathur

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