AU(III) AND CU(II) CATALYST FOR OXIDATION OF AROMATIC AND CYCLIC HYDROCARBON BY CERIUM (IV) IN ACIDIC MEDIUM UNDER MICROWAVE IRRADIATION

2016 ◽  
Vol 2 (4) ◽  
pp. 199
Author(s):  
Manish Srivastava ◽  
Ashu Goyal ◽  
Anamika Srivastava ◽  
Aakanksha Mishra ◽  
Preeti Tomar

The addition of traces of Au(III) chloride with Ce(IV) sulphate (catalyst: substrate ratio (1: 80 to 1: 300)) and in case of  Cu(II) sulphate with Ce(IV) sulphate(catalyst: substrate ratio (1: 60 to 1: 250)) in solution phase under microwave irradiation resulted in good to excellent yields of corresponding to phenol, quinone and carbonyl compounds. In case of  oxidation of anthracene, phenanthrene, naphthalene, cyclohexane and toluene dissolved in acetic acid to give 95.02 %, 85.25%, 34.68%, 40.94%, and 56.54% yields in case of gold catalyst and 93.5%, 83.4%, 24.68%, 38.25% and 47.11% yields in case of copper as a catalyst.  Phenanthrene was oxidized in 9-Fluorenone instead of phenanthraquinone to get the benzylic rearrangement.


1989 ◽  
Vol 54 (12) ◽  
pp. 3381-3386 ◽  
Author(s):  
Libor Havlíček ◽  
Jan Hanuš ◽  
Jan Němeček

The racemization rates of amino acids in acidic medium (acetic acid) were studied. The sensitivity to racemization decreases in the order (E)-3,4-didehydroornithine > (E)-Nδ-Z-3,4-didehydroornithine >> (Z)-3,4-didehydronorvaline > ornithine, norvaline. (E)-3,4-Didehydroornithine is also relatively rapidly racemized on heating with 5 M or 0.05 M-HCl (100 °C).



Author(s):  
Mousumi Chakraborty ◽  
Vaishali Umrigar ◽  
Parimal A. Parikh

The present study aims at assessing the effect of microwave irradiation against thermal heat on the production of N-acetyl-p-anisidine by acetylation of p-anisidine. The acetylation of p-anisidine under microwave irradiation produces N-acetyl-p-anisidine in shorter reaction times, which offers a benefit to the laboratories as well as industries. It also eliminates the use of excess solvent. Effects of operating parameters such as reaction time, feed composition, and microwave energy and reaction temperature on selectivity to the desired product have been investigated. The results indicate as high as a 98% conversion of N-acetyl-p-anisidine can be achieved within 12-15 minutes using acetic acid. The use of acetic acid as an acetylating agent against conventionally used acetic anhydride eliminates the handling of explosive acetic anhydride and also the energy intensive distillation step for separation of acetic acid. Organic solvent like acetic anhydride are not only hazardous to the environment, they are also expensive and flammable.



1987 ◽  
Vol 60 (11) ◽  
pp. 4143-4144 ◽  
Author(s):  
Takashi Morimoto ◽  
Masao Hirano ◽  
Hiroyuki Ashiya ◽  
Hidetaka Egashira ◽  
Xiumin Zhuang


ChemInform ◽  
2011 ◽  
Vol 42 (43) ◽  
pp. no-no
Author(s):  
Lalit Kumar Sharma ◽  
Kyung Bo Kim ◽  
Gregory I. Elliott


ChemInform ◽  
2010 ◽  
Vol 31 (34) ◽  
pp. no-no
Author(s):  
Majid M. Heravi ◽  
Dariush Ajami ◽  
Rahim Hekmatshoar ◽  
Yahya Sh. Beheshtiha ◽  
Karim Assadollah ◽  
...  


1997 ◽  
Vol 38 (17) ◽  
pp. 2959-2960 ◽  
Author(s):  
Didier Barbry* ◽  
Séverine Torchy


2014 ◽  
Vol 30 (2) ◽  
pp. 699-703 ◽  
Author(s):  
Hana Batmani ◽  
Davood Setamdideh


2003 ◽  
Vol 68 (10) ◽  
pp. 723-727 ◽  
Author(s):  
Vijay Dabholkar ◽  
Rahul Gavande

A series of 1-(3,4-dihydro-3-oxo-2H-1,4-benzoxazine-2-carbonyl)-3-methyl-4-(substituted phenylhydrazono)-2-pyrazolin-5-ones have been synthesized by the reaction of 2H-3,4-dihydro-3-oxo-1,4-benzoxazine-2-carboxylic acid hydrazide with substituted acetoacetic ester derivatives using acetic acid as solvent under microwave irradiation (MWI), as well as by conventional methods. The reaction rate is enhanced tremendously and the yields are improved under MWI as compared to conventional methods.



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