One-pot solvent-free microwave-assisted aza-Michael addition reaction of acrylonitrile

被引:6
|
作者
Das, Parineeta [1 ]
Devi, Nirmala [1 ]
Puzari, Amrit [1 ]
机构
[1] Natl Inst Technol Nagaland, Dept Chem, Chumoukedima, Dimapur 797103, Nagaland, India
关键词
Michael addition; Green chemistry; Molecular sieves; Di-adduct; Catalysis; EFFICIENT; CATALYST; AMINES; ACID; HETEROCYCLES; ZEOLITES;
D O I
10.1016/j.jics.2022.100411
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel and highly effective one-pot microwave-assisted aza-Michael addition reaction of acrylonitrile, as Michael acceptor with various primary aliphatic and aromatic amines, as Michael donor has been reported. The reaction was catalyzed by a cost-effective, highly efficient and eco-friendly catalyst, molecular sieve of 4 A(0) size, under solvent-free conditions. A detail investigation on reaction controlling parameters like reaction timing and amount of catalyst was studied. The plausible mechanistic pathway has been proposed for the formation of acrylonitrile adducts. The identity of the synthesized products was established by conventional spectroscopic techniques FT-IR, H-1 and C-13{H-1} NMR, ESI-MS and DLS measurements. DLS result shows hydrodynamic diameter of lower alkyl chain in the range of 200-300 nm and for higher alkyl chain around 1 mu m. Sheldon's hot filtration test confirms the significance of the catalyst and their heterogeneity was also confirmed by recycling it for five consecutive cycles without any noticeable change in the yield.
引用
收藏
页数:10
相关论文
共 50 条
  • [1] Microwave-Assisted, Rapid, Solvent-Free Aza-Michael Reaction by Perchloric Acid Impregnated on Silica Gel
    Singh, Surya Prakash
    Kumar, T. Vijaya
    Chandrasekharam, M.
    Giribabu, L.
    Reddy, P. Yella
    SYNTHETIC COMMUNICATIONS, 2009, 39 (22) : 3982 - 3989
  • [2] A microwave-assisted highly stereoselective one-pot Wittig reaction under solvent-free conditions
    Rajkumari, Kalyani
    Lama, Bittu
    Rokhum, Lalthazuala
    TURKISH JOURNAL OF CHEMISTRY, 2019, 43 (02) : 705 - 712
  • [3] Microwave-Assisted One-Pot Synthesis of Pyrazolone Derivatives under Solvent-Free Conditions
    Ma, Ruoqun
    Zhu, Jin
    Liu, Jie
    Chen, Lili
    Shen, Xu
    Jiang, Hualiang
    Li, Jian
    MOLECULES, 2010, 15 (05) : 3593 - 3601
  • [4] Microwave-assisted one-pot synthesis of α, β-unsaturated amides under solvent-free conditions
    Jiang, Shilei
    Xie, Yuanyuan
    Yu, Xiaochun
    JOURNAL OF CHEMICAL RESEARCH, 2009, (01) : 24 - 26
  • [5] Efficient Monoalkylation of Anilines with Chalcones using Microwave-Assisted aza-Michael Addition
    Iida, Hirokazu
    Okawa, Mitsuki
    Leeanansaksiri, Siriwat
    Takahashi, Kie
    LETTERS IN ORGANIC CHEMISTRY, 2022, 19 (08) : 608 - 615
  • [6] Solvent-free, catalyst-free aza-Michael addition of cyclohexylamine to diethyl maleate: Reaction mechanism and kinetics
    Blaha, Michal
    Trhlikova, Olga
    Podesva, Jiri
    Abbrent, Sabina
    Steinhart, Milos
    Dybal, Jiri
    Duskova-Smrckova, Miroslava
    TETRAHEDRON, 2018, 74 (01) : 58 - 67
  • [7] Microwave-assisted one-pot preparation of tetrahydro-β-carboline hydrochlorides under solvent-free conditions
    Liu, Fei
    You, Qi-Dong
    SYNTHETIC COMMUNICATIONS, 2007, 37 (22-24) : 3933 - 3938
  • [8] Microwave-assisted one-pot synthesis of α-fluoro-α,β-unsaturated esters under solvent-free conditions
    Ren, Aishan
    Yang, Xiongjun
    Hong, Jing
    Yu, Xiaochun
    SYNLETT, 2008, (15) : 2376 - 2378
  • [9] Amidation and Intramolecular Aza-Michael Reaction: One-Pot Synthetic Strategy of Isoindolinones
    Ali, Sk Asraf
    Bera, Anirban
    Molla, Mijanur Rahaman
    Samanta, Shubhankar
    CHEMISTRYSELECT, 2021, 6 (22): : 5603 - 5609
  • [10] Microwave-Assisted Organocatalytic Enantioselective Intramolecular aza-Michael Reaction with α,β-Unsaturated Ketones
    Fustero, Santos
    del Pozo, Carlos
    Mulet, Cristina
    Lazaro, Ruben
    Sanchez-Rosello, Maria
    CHEMISTRY-A EUROPEAN JOURNAL, 2011, 17 (50) : 14267 - 14272