Potassium Phosphate or Silica Sulfurc Acid Catalyzed Conjugate Addition of Thiols to α,β-Unsaturated Ketones at Room Temperature under Solvent-Free Conditions.

ChemInform ◽  
2007 ◽  
Vol 38 (14) ◽  
Author(s):  
D. M. Pore ◽  
M. S. Soudagar ◽  
U. V. Desai ◽  
T. S. Thopate ◽  
P. P. Wadagaonkar
Keyword(s):  
Room Temperature ◽  
Potassium Phosphate ◽  
Conjugate Addition ◽  
Solvent Free ◽  
Unsaturated Ketones ◽  
Solvent Free Conditions ◽  
Acid Catalyzed

Mandelic acid catalyzed one-pot three-component synthesis of α-aminonitriles and α-aminophosphonates under solvent-free conditions at room temperature

2020 ◽  
Vol 50 (10) ◽  
pp. 1545-1560 ◽  
Author(s):  
Gurpreet Kaur ◽  
Mussarat Shamim ◽  
Vaishali Bhardwaj ◽  
Vivek Kumar Gupta ◽  
Bubun Banerjee
Keyword(s):  
Mandelic Acid ◽  
Room Temperature ◽  
Solvent Free ◽  
One Pot ◽  
Solvent Free Conditions ◽  
Acid Catalyzed

scholarly journals Solvent-free synthesis of enantioenriched β-silyl nitroalkanes under organocatalytic conditions

2021 ◽  
Vol 17 ◽  
pp. 2642-2649
Author(s):  
Akhil K Dubey ◽  
Raghunath Chowdhury
Keyword(s):  
Temperature Control ◽  
Carbonyl Compounds ◽  
Room Temperature ◽  
Conjugate Addition ◽  
High Reactivity ◽  
Solvent Free ◽  
Reaction Conditions ◽  
Silyl Group ◽  
Solvent Free Conditions ◽  
Solvent Free Synthesis

An enantioselective 1,4-conjugate addition of nitromethane to β-silyl α,β-unsaturated carbonyl compounds catalyzed by bifunctional squaramide catalysts has been developed. This methodology offers both enantiomers of β-silyl nitroalkanes in good to excellent yields (up to 92%) and enantioselectivities (up to 97.5% ee) under solvent-free conditions at room temperature. Control experiments reveal that the presence of a β-silyl group in the enones is crucial for high reactivity under the optimized reaction 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.

scholarly journals Tandem Fries Reaction–Conjugate Addition under Microwave Irradiation in Dry Media; One-pot Synthesis of Flavanones

1999 ◽  
Vol 23 (9) ◽  
pp. 574-575
Author(s):  
Firouz Matloubi Moghaddam ◽  
Mohammad Ghaffarzadeh ◽  
Seyed Hossein Abdi-Oskoui
Keyword(s):  
Microwave Irradiation ◽  
Silica Gel ◽  
Conjugate Addition ◽  
Solvent Free ◽  
Naphthalene Derivatives ◽  
One Pot ◽  
Fries Rearrangement ◽  
One Pot Synthesis ◽  
Solvent Free Conditions ◽  
Fries Reaction

An AICl3–ZnCl2 mixture supported on silica gel is found to be an efficient medium for the Fries rearrangement of acyloxybenzene or naphthalene derivatives in solvent-free conditions under microwave irradiation.

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

Synthesis of 1,1-diacetates from Aromatic Aldehydes using Cerium(IV) Sulfate Tetrahydrate as Catalyst under Solvent-free Conditions

2005 ◽  
Vol 2005 (3) ◽  
pp. 171-172 ◽  
Author(s):  
Min Zhang ◽  
Yi-Qun Li
Keyword(s):  
Room Temperature ◽  
Aromatic Aldehydes ◽  
Solvent Free ◽  
Excellent Yield ◽  
Solvent Free Conditions

Aromatic aldehydes can be converted into the corresponding 1,1-diacetates rapidly in the presence of catalytic amounts of Ce(SO4)2·4H2O at room temperature in excellent yield under solvent-free conditions. The catalyst can easily be recovered and reused at least 4 times.

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