Micro-Cu4I4-MOF: reversible iodine adsorption and catalytic properties for tandem reaction of Friedel–Crafts alkylation of indoles with acetals

2016 ◽  
Vol 52 (86) ◽  
pp. 12702-12705 ◽  
Author(s):  
Neng-Xiu Zhu ◽  
Chao-Wei Zhao ◽  
Jian-Cheng Wang ◽  
Yan-An Li ◽  
Yu-Bin Dong
Keyword(s):  
Heterogeneous Catalyst ◽  
Room Temperature ◽  
Catalytic Properties ◽  
Solvent Free ◽  
Tandem Reaction ◽  
Solvent Free Conditions ◽  
Iodine Adsorption

I2@Cu4I4-MOF can be a highly heterogeneous catalyst to promote the tandem reaction of Friedel–Crafts alkylation of indoles with acetals under solvent-free conditions at room temperature.

An efficient method for the silylation of hydroxyl groups with hexamethyldisilazane (HMDS) catalyzed by aluminum tris(dihydrogen phosphate) under solvent-free and ambient conditions

2008 ◽  
Vol 86 (8) ◽  
pp. 841-845 ◽  
Author(s):  
Hamid Reza Shaterian ◽  
Majid Ghashang ◽  
Nassrin Tajbakhsh Riki ◽  
Manijeh Asadi
Keyword(s):  
Heterogeneous Catalyst ◽  
Efficient Method ◽  
Room Temperature ◽  
Solvent Free ◽  
Dihydrogen Phosphate ◽  
Hydroxyl Groups ◽  
Ambient Conditions ◽  
Solvent Free Conditions ◽  
Free Hydroxyl ◽  
Recyclable Heterogeneous Catalyst

A highly efficient and mild procedure for the trimethylsilylation of a wide variety of alcohols, including primary, benzylic, secondary, hindered secondary, tertiary, phenols, and oximes with hexamethyldisilazane (HMDS), using Al(H2PO4)3 as a recyclable heterogeneous catalyst at room temperature in a few minutes with excellent yields under solvent-free conditions is described.Key words: trimethylsilylation, hexamethyldisilazane, aluminum tris(dihydrogen phosphate) [Al(H2PO4)3], solvent-free, hydroxyl groups.

scholarly journals Acetylation of Phenols, Anilines, and Thiols Using Silica Sulfuric Acid under Solvent-Free Conditions

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Davood Habibi ◽  
Payam Rahmani ◽  
Ziba Akbaripanah
Keyword(s):  
Sulfuric Acid ◽  
Heterogeneous Catalyst ◽  
Room Temperature ◽  
Solvent Free ◽  
Amino Group ◽  
Silica Sulfuric Acid ◽  
Solvent Free Conditions

Silica sulfuric acid was employed as a heterogeneous catalyst for the acetylation of a variety of phenols, amines, and thiols under solvent-free conditions at room temperature. Deactivated substrates also acetylated rapidly, and the method showed the preferential selectivity for acetylation of amino group in the presence of hydroxyl groupinwhich no C-acylation was observed.

PMA/SiO2 – An efficient recyclable heterogeneous catalyst for the synthesis of homoallyl alcohols and amines under solvent-free conditions

2008 ◽  
Vol 86 (7) ◽  
pp. 709-713 ◽  
Author(s):  
Biswanath Das ◽  
Rathod Aravind Kumar ◽  
Ponnaboina Thirupathi ◽  
Kanaparthy Suneel ◽  
Pothkan Sunitha
Keyword(s):  
Heterogeneous Catalyst ◽  
Nucleophilic Addition ◽  
Room Temperature ◽  
Addition Reaction ◽  
Phosphomolybdic Acid ◽  
Solvent Free ◽  
Solvent Free Conditions ◽  
Nucleophilic Addition Reaction ◽  
Recyclable Heterogeneous Catalyst

Aldehydes and imines can efficiently undergo nucleophilic addition reaction with allyltributylstannane in the presence of phosphomolybdic acid supported on silica (PMA/SiO2) under solvent free-conditions to form the corresponding homoallyl alcohols and amines respectively at room temperature in excellent yields. The catalyst can be easily recovered and re-used.Key words: homoallyl alcohol, homoallyl amine, phosphomolybdic acid, heterogeneous catalyst, allyltributylstannane, solvent-free conditions.

Preparation and Characterization of a Novel Room Temperature Dicationic Ionic Liquid and its Application in the Synthesis of Xanthenediones Under Solvent-Free Conditions

2018 ◽  
Vol 21 (8) ◽  
pp. 602-608 ◽  
Author(s):  
Zainab Ehsani-Nasab ◽  
Ali Ezabadi
Keyword(s):  
Ionic Liquid ◽  
Room Temperature ◽  
Reaction Times ◽  
Significant Loss ◽  
Solvent Free ◽  
Acidity Function ◽  
Efficient Catalyst ◽  
Solvent Free Conditions ◽  
Hammett Acidity Function ◽  
Dicationic Ionic Liquid

Aim and Objective: In the present work, 1, 1’-sulfinyldiethylammonium bis (hydrogen sulfate) as a novel room temperature dicationic ionic liquid was synthesized and used as a catalyst for xanthenediones synthesis. Material and Method: The dicationic ionic liquid has been synthesized using ethylamine and thionyl chloride as precursors. Then, by the reaction of [(EtNH2)2SO]Cl2 with H2SO4, [(EtNH2)2SO][HSO4]2 was prepared and after that, it was characterized by FT-IR, 1H NMR, 13C NMR as well as Hammett acidity function. This dicationic ionic liquid was used as a catalyst for the synthesis of xanthenediones via condensation of structurally diverse aldehydes and dimedone under solvent-free conditions. The progress of the reaction was monitored by thin layer chromatography (ethyl acetate/n-hexane = 3/7). Results: An efficient solvent-free method for the synthesis of xanthenediones has been developed in the presence of [(EtNH2)2SO][HSO4]2 as a powerful catalyst with high to excellent yields, and short reaction times. Additionally, recycling studies have demonstrated that the dicationic ionic liquid can be readily recovered and reused at least four times without significant loss of its catalytic activity. Conclusion: This new dicationic ionic liquid can act as a highly efficient catalyst for xanthenediones synthesis under solvent-free conditions.

Efficient Synthesis of Tetrahydrobenzo[b]pyrans under Solvent‐Free Conditions at Room Temperature

2006 ◽  
Vol 36 (16) ◽  
pp. 2363-2369 ◽  
Author(s):  
Liangce Rong ◽  
Xiaoyue Li ◽  
Haiying Wang ◽  
Daqing Shi ◽  
Shujiang Tu ◽  
...  
Keyword(s):  
Room Temperature ◽  
Solvent Free ◽  
Efficient Synthesis ◽  
Solvent Free Conditions
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