2169-68-8Relevant articles and documents
Minimizing solvent waste in catalytic reactions in highly recyclable hydrocarbon solvents
Bergbreiter, David E.,Killough, James M.,Thavornpradit, Sopida
, p. 4248 - 4256 (2020)
This paper describes chemistry using organocatalysts in hydrocarbon solvents that minimizes solvent waste by using inexpensive, non-volatile, relatively inflammable, and easily recyclable poly(α-olefin)s (PAOs) as hydrocarbon solvents. These studies show that when substrates have limited solubility in PAO solvents, this issue can be addressed by adding a small amount of a cosolvent. Kinetic studies were also carried out and show that reactions carried out in PAOs are kinetically comparable to reactions in conventional non-recyclable hydrocarbon solvents. A range of strategies that separate and isolate products from reactions in PAOs using a polyisobutylene (PIB)-supported DMAP catalyst have been studied using four different catalytic reactions. In the most general procedure, the PAO phase containing a PIB-bound catalyst is separated from products by low energy liquid/liquid gravity separation. This can be accomplished using a minimal amount of a polar solvent. In another example, the product's low solubility leads to it precipitating during the reaction. In this case, a simple filtration recycles the PAO and a PIB-bound DMAP catalyst. We have demonstrated that the PAO phase containing a PIB bound DMAP catalyst can be recycled for at least 10 cycles without loss of activity. Our studies further showed that leaching of the PAO phase into polar solvents was orders of magnitude less than conventional hydrocarbon solvents such as heptane. The result is that the overall solvent waste generation is lower than for the same reaction carried out in conventional solvents.
Ammonium chloride catalyzed Knoevenagel condensation in PEG-400 as ecofriendly solvent
Waghmare, Smita R.
, p. 849 - 855 (2021/09/28)
A simple and selective green methodology has been successfully developed for Knoevenagel condensation in polyethylene glycol-400 using 10 mol % ammonium chloride as catalyst. The method is applicable to a wide range of aromatic, heteroaromatic and α,β-unsaturated aldehydes. The reactions have been found to be clean and free from the formation of the Michael adduct.
Silica bonded N-(propylcarbamoyl)sulfamic acid (SBPCSA) as a highly efficient and recyclable solid catalyst for the synthesis of Benzylidene Acrylate derivatives: Docking and reverse docking integrated approach of network pharmacology
Aslam, Afroz,Parveen, Mehtab,Alam, Mahboob,Silva, Manuela Ramos,Silva, P.S. Pereira
, (2020/08/17)
A green approach has been developed for the synthesis of a series of benzylidene acrylate 3(a-p) from differently substituted aromatic/heterocyclic aldehydes and ethyl cyanoacetate in excellent yields (90–98%), and employing silica bonded N-(Propylcarbamoyl)sulfamic acid as a recyclable catalyst under solvent-free condition. The molecular structure of compounds 3b, 3d and 3i were well supported by single-crystal X-ray crystallographic analysis. The present protocol bears wide substrate tolerance and is believed to be more practical, efficient, eco-friendly, and compatible as compared to existing methods. In-silico approaches were implemented to find the biochemical and physiological effects, toxicity, and biological profiles of the synthesized compounds to determine the expected biological nature and confirm a drug-like compound. A molecular docking study of the expected biologically active compound was performed to know the hypothetically binding mode with the receptor. Also, reverse docking is applied to recognize receptors from unknown protein targets for drug-like compounds to explain poly-pharmacology and binding postures with different receptors.
The Modified Clay as a New and Eco-Friendly Catalyst for the Knoevenagel Reaction
Bentahar, S.,Dbik, A.,Khomri, M. El,Lacherai, A.,Messaoudi, N. El,Sabour, A.,Taleb, M. Ait
, p. 1438 - 1444 (2020/10/29)
Abstract: This work aims the synthesis of substituted alkenes via Knoevenagel condensation using the clay collected from the Agadir region and modified by KF as a heterogeneous catalyst (KF-modified clay). In this context, the influence of various paramet
Selenotungstates incorporating organophosphonate ligands and metal ions: synthesis, characterization, magnetism and catalytic efficiency in the Knoevenagel condensation reaction
Ban, Ran,He, Peipei,Kong, Hui,Ma, Pengtao,Niu, Jingyang,Wang, Jiawei,Wang, Jingping,Xu, Qiaofei,Yang, Zongfei
supporting information, p. 7420 - 7425 (2020/06/21)
Three sandwich-type TM-containing (TM = transition metal) organophosphonate-based polyoxotungstate clusters, [TM(H2O)4(SeW6O21)2{Co(OOCCH2NCH2PO3)2}3]12?(TM = Co, Ni), have been successfully synthesized, which are the first reported TM-containing organophosphonate-based selenotungstates. They were structurally characterized by PXRD analyses, IR spectroscopy, TGA analyses,etc. Magnetic measurements show that all three compounds exhibit antiferromagnetic interactions. Besides,Co1can be used as an efficient heterogeneous catalyst in the Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate under mild conditions (60 °C), and exhibits satisfactory conversion (93%) and high selectivity (99%).
Molybdenum oxide nanoparticles as recyclable heterogeneous catalyst for synthesis of arylidene ethyl cyanoacetates
Pourshojaei, Yaghoub,Eskandari, Khalil,Elhami, Elaheh,Asadipour, Ali
, p. 5965 - 5973 (2019/06/14)
This work reports an adapted route to the highly efficient synthesis of arylidene ethyl cyanoacetate derivatives in the presence of catalytic amounts of molybdenum oxide nanoparticles (MoO3 NPs) under green conditions at ambient temperature. From the reaction, a wide range of novel arylidene ethyl cyanoacetates was successfully synthesized with high yields from the Knoevenagel condensation reaction between various aryl aldehydes and ethyl cyanoacetate in the presence of MoO3 nanoparticles. The capability of catalyst to separate from the reaction mixture and then reuse is another advantage of this reaction. Furthermore, obtained products belong to analogous of organic compounds that have shown biological activity, and can be used pharmaceutics.
Amino Acid Amide based Ionic Liquid as an Efficient Organo-Catalyst for Solvent-free Knoevenagel Condensation at Room Temperature
Burate, Pralhad A.,Javle, Balasaheb R.,Desale, Pranjal H.,Kinage, Anil K.
, p. 2368 - 2375 (2019/06/17)
Abstract: Ionic liquids of amino acid amide were synthesized and used as an efficient catalyst for solvent-free Knoevenagel condensation. Synthesized ionic liquids are an environmentally benign, inexpensive, metal free and plays the dual role of solvent as well as an efficient catalyst for Knoevenagel condensation. A wide range of aliphatic, aromatic and heteroaromatic aldehydes easily undergo condensation with malononitrile and ethyl cyanoacetate. The reaction proceeds at room temperature without using any organic solvent and is very fast with good to excellent yield. Additionally, the catalyst is easily separable and recyclable without loss of activity. Graphic Abstract: [Figure not available: see fulltext.].
The Knoevenagel condensation using quinine as an organocatalyst under solvent-free conditions
Jain, Kavita,Chaudhuri, Saikat,Pal, Kuntal,Das, Kalpataru
supporting information, p. 1299 - 1304 (2019/01/21)
The Knoevenagel condensation between active methylene compounds and aromatic carobonyl compounds has been developed using quinine as an organocatalyst to afford various electrophilic alkenes in excellent yields (up to 90%). In the presence of a catalytic amount of quinine (15 mol%), the reaction proceeded at room temperature (RT) under solvent-free conditions. In this green approach, the organocatalyst was recovered and recycled for up to four cycles without appreciable loss of activity.
Hypervalent Iodine(III)-Catalyzed Epoxidation of β-Cyanostyrenes
Mangaonkar, Saeesh R.,Singh, Fateh V.
, p. 4473 - 4486 (2019/11/21)
A convenient approach for the synthesis of β-cyanoepoxides is illustrated by iodine(III)-catalyzed epoxidation of electron-deficient β-cyanostyrenes, wherein the active catalytic iodine(III) species was generated in situ. The epoxidation of β-cyanostyrenes was performed using 10 molpercent PhI as precatalyst in the presence of 2.0 equivalents Oxone as an oxidant and 2.4 equivalents of TFA as an additive at room temperature under ultrasonic radiations. The β-cyanoepoxides were isolated in good to excellent yields in a short reaction time.
A functionalized UiO-66 MOF for turn-on fluorescence sensing of superoxide in water and efficient catalysis for Knoevenagel condensation
Das, Aniruddha,Anbu, Nagaraj,Sk, Mostakim,Dhakshinamoorthy, Amarajothi,Biswas, Shyam
, p. 17371 - 17380 (2019/12/02)
In the present work, a new MOF material of the UiO-family called Zr-UiO-66-NH-CH2-Py (1) has been obtained by the solvothermal technique and successfully characterized. The MOF structure was assembled with 2-((pyridin-4-ylmethyl) amino) terephthalic acid (H2BDC-NH-CH2-Py) as linker and Zr4+ ion. The activated form of 1 (called 1′) exhibits considerable thermal and chemical stability. Compound 1′ showed a very rapid and selective response for the fluorometric sensing of superoxide (O2·-) in aqueous medium even in the presence of the potentially competitive reactive oxygen species (ROS). The limit of detection value for O2·- sensing is 0.21 μM, which is comparable with those of the reported O2·- sensors. This is the first MOF based fluorescent sensor for the detection of O2·-. The response time of this MOF sensor for O2·- is very short (240 s). On the other hand, 1′ was employed as a solid heterogeneous catalyst for Knoevenagel condensation between benzaldehyde and ethyl cyanoacetate at 80 °C in ethanol resulting in a very high yield of the desired product. The effects of the esterified linker ((CH3)2BDC-NH-CH2-Py) and the corresponding metal salt (ZrCl4) on this catalytic reaction were examined separately. We have also tested the substrate scope elaborately for the catalytic reaction promoted by catalyst 1′.
