scholarly journals P2O5/SiO2as a New, Efficient and Reusable Catalyst for Preparation of 4,4′-Epoxydicoumarins Under Solvent-free Conditions

2011 ◽  
Vol 8 (4) ◽  
pp. 1626-1631 ◽  
Author(s):  
Liqiang Wu ◽  
Xiao Wang
Keyword(s):  
Silica Gel ◽  
Low Cost ◽  
Reaction Times ◽  
Catalytic Amount ◽  
Phosphorus Pentoxide ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
Solvent Free Conditions ◽  
High Yields

An efficient solvent-free procedure for the preparation of 4,4′-epoxydicoumarins via the ondensation of 4-hydroxycoumarin with aldehydes in the presence of catalytic amount of phosphorus pentoxide/silica gel at 110°C is described. The advantages of this method are generality, high yields, short reaction times, ease of product isolation, low cost and ecologically friendly.

Rapid and Green One-Pot Synthesis of Novel 2-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-2-(arylamino)-1H-indene-1,3(2H)-diones

2021 ◽  
Vol 18 ◽  
Author(s):  
Abolfazl Olyaei ◽  
Zahra Ghahremany ◽  
Madieh Sadeghpour
Keyword(s):  
Aromatic Amines ◽  
Low Cost ◽  
Guanidine Hydrochloride ◽  
Reaction Times ◽  
Solvent Free ◽  
One Pot ◽  
Solvent Free Conditions ◽  
The One ◽  
High Yields ◽  
Work Up

: A green and efficient protocol was developed for the one-pot three-component synthesis of novel 2-(4-hydroxy-2-oxo-2H-chromen-3-yl)-2-(arylamino)-1H-indene-1,3(2H)-dione derivatives by the reaction of 4-hydroxycoumarin, ninhydrin and aromatic amines in the presence of guanidine hydrochloride as an organocatalyst under solvent-free conditions. The present approach offers several advantages such as low cost, simple work-up, short reaction times, chromatography-free purification, high yields and greener conditions.

scholarly journals Fe3o4 nanoparticles: A highly efficient and easily reusable catalyst for the one-pot synthesis of xanthene derivatives under solvent-free conditions

2013 ◽  
Vol 78 (6) ◽  
pp. 769-779 ◽  
Author(s):  
Ali Ghasemzadeh ◽  
Javad Safaei-Ghomi ◽  
Safura Zahedi
Keyword(s):  
Fe3o4 Nanoparticles ◽  
Reaction Times ◽  
Aromatic Aldehydes ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
One Pot ◽  
Solvent Free Conditions ◽  
Xanthene Derivatives ◽  
The One ◽  
High Yields

Magnetically separable Fe3O4 nanoparticles supply environmentally friendly procedure for the synthesis of 14-aryl-14H-dibenzo[a,j]xanthene and 1,8-dioxo-octahydro-xanthene derivatives. These compounds were obtained in high yields and short reaction times by the reaction of dimedone and 2-naphthol with various aromatic aldehydes under solvent-free conditions. The catalyst coluld be easily recovered using an external magnet and reused for six cycles with almost consistent activity.

Synthesis of 3-Aryl-Benzo[b]Furans and 3-Aryl-Naphtho[b]Furans Using N-Propyl-4-Aza-1-Azoniabicyclo[2.2.2]Octane Chloride Immobilised on SiO2 as an Efficient and Reusable Catalyst

2018 ◽  
Vol 42 (2) ◽  
pp. 86-89 ◽  
Author(s):  
Mohammad Akrami Abarghooei ◽  
Razieh Mohebat ◽  
Zahed Karimi-Jaberi ◽  
Mohammad Hossein Mosslemin
Keyword(s):  
Convenient Method ◽  
Reaction Times ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
Solvent Free Conditions ◽  
High Yields

A new and convenient method is describe d for the synthesis of 3-aryl-benzo[ b]furans and 3-aryl-naphtho[ b]furans by the reaction of various α-bromoketones with phenols and 2-naphthols in the presence of n-propyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride immobilised on SiO2. All products were obtained in high yields and short reaction times using solvent-free conditions and a reusable catalyst.

A solvent-free protocol for facile condensation of indoles with carbonyl compounds using silica chloride as a new, highly efficient, and mild catalyst

2007 ◽  
Vol 85 (6) ◽  
pp. 416-420 ◽  
Author(s):  
Alireza Hasaninejad ◽  
Abdolkarim Zare ◽  
Hashem Sharghi ◽  
Mohsen Shekouhy ◽  
Reza Khalifeh ◽  
...  
Keyword(s):  
Carbonyl Compounds ◽  
Electrophilic Substitution ◽  
Room Temperature ◽  
Low Cost ◽  
Reaction Times ◽  
Catalytic Amount ◽  
Solvent Free ◽  
Substitution Reactions ◽  
Aldehydes And Ketones ◽  
High Yields

A simple and efficient solvent-free procedure for the preparation of bis(indolyl)methanes via electrophilic substitution reactions of indoles with aldehydes and ketones is described. The reactions took place in the presence of a catalytic amount of silica chloride at room temperature. The advantages of this method are high yields, short reaction times, low cost, and compliance with green-chemistry protocols.Key words: silica chloride, indole, carbonyl compound, solvent-free, bis(indolyl)methane.

A Facile and Efficient Conversion of Aldehydes into 1,1-Diacetates (Acylals) using Iron(III) Fluoride as a Novel Catalyst

2007 ◽  
Vol 60 (8) ◽  
pp. 590 ◽  
Author(s):  
V. T. Kamble ◽  
R. A. Tayade ◽  
B. S. Davane ◽  
K. R. Kadam
Keyword(s):  
Large Scale ◽  
Room Temperature ◽  
Reaction Times ◽  
Catalytic Amount ◽  
Solvent Free ◽  
Present System ◽  
Efficient Conversion ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Novel Catalyst

Aldehydes are smoothly converted into the corresponding 1,1-diacetates (acylals) in high yields in the presence of a catalytic amount (0.1 mol-%) of iron(III) fluoride at room temperature. The noteworthy features of the present system are shorter reaction times, chemoselective protection of aldehydes, and solvent-free conditions. The procedure is especially useful for large-scale syntheses as the catalyst is highly effective from the view of activity, selectivity, reusability, and economy in the preparation of 1,1-diacetates (acylals).

scholarly journals Molybdenum Oxide Supported on Silica (MoO /SiO ): An Efficient and Reusable Catalyst for the Synthesis of 1,8-dioxodecahydroacridines Under Solvent-free Conditions

2017 ◽  
Vol 59 (1) ◽  
Author(s):  
Amir Khojastehnezhad
Keyword(s):  
Molybdenum Oxide ◽  
Ammonium Acetate ◽  
Reaction Times ◽  
Aromatic Aldehydes ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Work Up ◽  
Considerable Loss

Silica supported molybdenum oxide (MoO<sub>3</sub>/SiO<sub>2</sub>) was found to be an efficient, eco-friendly and heterogeneous catalyst for the multicomponent reaction of aromatic aldehydes, dimedone and ammonium acetate or aromatic amines under solvent-free conditions to afford the corresponding 1,8-dioxodecahydroacridines  in high yields. The catalyst can be easily recovered and reused for several times without considerable loss of activity. Furthermore, the present method offers several advantages, such as an easy experimental and work-up procedures, short reaction times and good to excellent yields.

A highly efficient and green approach for the synthesis of pyrimido[4,5-b]quinolines using N,N-diethyl-N-sulfoethanaminium chloride

2021 ◽  
Vol 76 (2) ◽  
pp. 85-90
Author(s):  
Abdolkarim Zare ◽  
Manije Dianat
Keyword(s):  
Reaction Times ◽  
Solvent Free ◽  
One Pot ◽  
Catalyst Amount ◽  
Green Protocol ◽  
Highly Efficient ◽  
Green Approach ◽  
Solvent Free Conditions ◽  
The One ◽  
High Yields

Abstract A highly efficient and green protocol for the synthesis of pyrimido[4,5-b]quinolines has been described. The one-pot multicomponent reaction of dimedone with arylaldehydes and 6-amino-1,3-dimethyluracil in the presence of N,N-diethyl-N-sulfoethanaminium chloride ([Et3N–SO3H][Cl]) as an ionic liquid (IL) catalyst under solvent-free conditions afforded the mentioned compounds in high yields and short reaction times. Our protocol is superior to many of the reported protocols in terms of two or more of these factors: the reaction times, yields, conditions (solvent-free versus usage of organic solvents), temperature and catalyst amount.

scholarly journals Synthesis and Characterization of Functionalize HY Zeolite With Sulfunic Acid, A Micro-meso Structure as an Efficient Reusable Catalyst in Organic Transformations

2021 ◽  
Author(s):  
Mojgan Zendehdel ◽  
Fatemeh Tavakoli
Keyword(s):  
Reaction Times ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
Organic Transformations ◽  
Hy Zeolite ◽  
New Class ◽  
Solvent Free Condition ◽  
Result Show ◽  
High Yields

Abstract A new class of catalyst has been prepared with sulfunic acid functionalized HY zeolite (HY-N-SO3H) and characterized by FESEM, TEM, FTIR, TGA, XRD and BET. The result show that the catalyst has the micro-meso structure without ordering in the mesophase. Then, two sets of organic reaction were examined to consider of catalytic activity. The micro-meso structure HY-N-SO3H was used as an acidic catalyst to synthesis of coumarins via Pechmann reaction and facile transformation of amines to formamides under solvent free condition. This catalyst was compared with NaY-N-SO3H and MCM-N-SO3H and pure porous material to consider of the effect of acidity and kind and size of porous in the catalyst. The significant advantages of HY-N-SO3H respect to other catalyst are short reaction times, high yields, pure products, mild conditions and easy workup. In addition, we report an original and environmentally friendly solvent-free procedures which reusability of catalyst makes this method nearly green and environmental friendly.

A One-Pot, Three-Component, Solvent-Free Synthesis of Novel 6H-Chromeno[3’,4’:5,6]Pyrido[2,3-d]Pyrimidine-Triones under Microwave Irradiation

2018 ◽  
Vol 42 (12) ◽  
pp. 604-607
Author(s):  
Loghman Firoozpour ◽  
Hoda Yahyavi ◽  
Ramona Ejtemaei ◽  
Setareh Moghimi ◽  
Alireza Foroumadi
Keyword(s):  
Microwave Irradiation ◽  
Efficient Method ◽  
Barbituric Acid ◽  
Reaction Times ◽  
Solvent Free ◽  
One Pot ◽  
Solvent Free Conditions ◽  
Substituted Benzaldehydes ◽  
High Yields ◽  
Solvent Free Synthesis

A green and efficient method for preparing novel heterocyclic systems is established through the reaction of differently substituted benzaldehydes, barbituric acid and 4-amino-2H-chromene-2-one under solvent-free conditions. This method affords 6H-chromeno[3’,4’:5,6] pyrido[2,3-d]pyrimidine-trione derivatives in high yields and short reaction times.

scholarly journals A Solvent-Free Protocol for the Green Synthesis of 5-Arylidene-2,4-thiazolidinediones Using Ethylenediamine Diacetate as Catalyst

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Yuliang Zhang ◽  
Zhongqiang Zhou
Keyword(s):  
Knoevenagel Condensation ◽  
Aromatic Aldehydes ◽  
Solvent Free ◽  
Reusable Catalyst ◽  
Efficient Synthesis ◽  
Reaction Conditions ◽  
Solvent Free Conditions ◽  
High Yields ◽  
Work Up ◽  
Solvent Free Reaction

A simple and efficient synthesis of 5-arylidene-2,4-thiazolidinediones by the Knoevenagel condensation of aromatic aldehydes with 2,4-thiazolidinedione catalyzed by ethylenediamine diacetate under solvent-free conditions is described. The major advantages of this method are simple experimental and work-up procedures, solvent-free reaction conditions, small amount of catalyst, short reaction time, high yields, and utilization of an inexpensive and reusable catalyst.

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