Silica sulfuric acid-catalyzed expeditious environment-friendly hydrolysis of carboxylic acid esters under microwave irradiation

2008 ◽  
Vol 62 (6) ◽  
Author(s):  
Zheng Li ◽  
Jing Liu ◽  
Xue Gong ◽  
Xuerong Mao ◽  
Xiunan Sun ◽  
...  

AbstractSilica sulfuric acid was found to be an efficient, recoverable, reusable and environment-friendly catalyst for the fast hydrolysis of various carboxylic acid esters in high conversions and selectivities under microwave irradiation conditions. This protocol has the advantages of no corrosion, no environmental pollution, high reaction rate, high yield, and simple work-up procedure.

1971 ◽  
Vol 49 (17) ◽  
pp. 2797-2802 ◽  
Author(s):  
D. E. Horning ◽  
G. Lacasse ◽  
J. M. Muchowski

The sulfuric acid catalyzed acylation of 2-methyl-5-nitroisocarbostyril with carboxylic acid anhydrides gave the corresponding 4-acylated derivatives 3, which underwent reductive cyclization to 2-substituted derivatives of 4-methyl-1,3,4,5-tetrahydropyrrolo[4.3.2.de]isoquinolin-5-one (4). Alkaline hydrolysis of the six-membered lactam in 4 was accompanied by a retro-Mannich reaction to produce 2-substituted indole-4-carboxylic acids in about 40 % overall yield from 3.


2012 ◽  
Vol 9 (5) ◽  
pp. 791-798 ◽  
Author(s):  
R. Ghanbaripour ◽  
I. Mohammadpoor-Baltork ◽  
M. Moghadam ◽  
A. R. Khosropour ◽  
S. Tangestaninejad ◽  
...  

1984 ◽  
Vol 62 (9) ◽  
pp. 1840-1844 ◽  
Author(s):  
Karl R. Kopecky ◽  
Alan J. Miller

Treatment of methyl hydrogen decahydro-1,4:5,8-exo,endo-dimethanonaphthalene-4a,8a-dicarboxylate with lead tetraacetate in benzene – acetic acid replaces the carboxyl group by an acetoxy group. Hydrolysis of this product with 25% sulfuric acid at 130 °C forms 8a-hydroxydecahydro-1,4:5,8-exo,endo-dimethanonaphthalene-4a-carboxylic acid 10. The reaction between 10 and benzenesulfonyl chloride in pyridine containing triethylamine at 95 °C produces anti-sesquinorbornene 1 in 34% yield. In the absence of triethylamine 1 is converted to the hydrochloride. The iodohydroperoxide of 1 is converted by silver acetate at 0 °C to the diketone in a luminescent reaction. The 1,2-dioxetane could not be isolated. Decahydro-1,4:5,8-exo,exo-dimethanonaphthalene-4a,8a-dicarboxylic anhydride is converted slowly by methoxide ion in methanol at 150 °C to the monomethyl ester which then undergoes demethylation. The isomeric exo,endo anhydride undergoes reaction readily with methoxide ion at 80 °C.


2003 ◽  
Vol 24 (1) ◽  
pp. 97-101 ◽  
Author(s):  
Jiaqing Xie ◽  
Yi Zhang ◽  
Juan Du ◽  
Xian‐cheng Zeng ◽  
Ying‐jin Liu ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Bahareh Sadeghi ◽  
Tayebe Ziya

Silica sulfuric acid nanoparticles have been prepared and shown to efficiently catalyse the reaction between an aromatic aldehyde or phenylglyoxal and a 4-hydroxycoumarin at reflux in EtOH to afford the biscoumarin derivatives in high yield.


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