Araştırma Makalesi

Microwave-Assisted Synthesis of Acyclic Imides

Cilt: 12 Sayı: 1 1 Mart 2022
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Microwave-Assisted Synthesis of Acyclic Imides

Öz

Imides are an important class of compounds found in the structure of many biologically active and natural compounds. Imides are also important starting materials used in the synthesis of many heterocyclic compounds. Therefore, the synthesis of these compounds has attracted considerable attention and several innovative methods have been developed. Herein, the synthesis of acyclic imides has been reported from nitriles and carboxylic anhydrides in the presence of catalytic amounts of p-toluenesulfonic acid (PTSA) or H2SO4 under microwave irradiation. The reaction has proceeded in better yields with PTSA. When sulfuric acid was used, the product was obtained in lower yields since the degradation was increased. This new microwave-assisted method is compared with conventional heating, and the other methods, reported in the literature. The main advantages of this procedure are shorter reaction times, easier work-up, and good yields.

Anahtar Kelimeler

Kaynakça

  1. Aruri H., Singh U., Kumar S., Kushwaha M., Gupta A. P., Vishwakarma R. A., Singh P. P., 2016. I2/Aqueous TBHP-catalyzed coupling of amides with methylarenes/ aldehydes/alcohols: Metal-Free synthesis of imides. Org. Lett., 18: 3638-3641.
  2. Atanassova I.A., Petrov J.S., Ognjanova V.H., Mollov N.M., 1990. α,α,α-Trichloroketrylcarbonyl compounds as acylating reagents of amides. Synth. Commun., 20: 2083-2090.
  3. Bates R.B., Fletcher F.A., Janda K.D., Miller W.A. 1984. A convenient synthesis of unsymmetrical acyclic imides. J. Org. Chem., 49: 3038.
  4. Challis B.C., Challis J., Zabicky J. (Ed.). 1970. The chemistry of amides. pp 759, J. Wiley and Sons, New York,
  5. Davidson, D., Skovronek H. 1958. The acylation of amides. J. Am. Chem. Soc., 80 (2): 376-379.
  6. Ding G., Jiang L., Guo L., Chen X., Zhang H., Che Y. 2008. Pestalazines and pestalamides, bioactive metabolites from the plant pathogenic fungus pestalotiopsis theae. J. Nat. Prod., 71: 1861-1865.
  7. Durrell W.S., Young J.A., Dresdner R.D. 1963. Fluorocarbon nitrogen compounds. IX. The reaction of nitriles with carboxylic acids. J. Org. Chem., 28: 831-833.
  8. Flitsch W., Hohenhorst M. 1990. N‐Protected 3‐hydroxypyrroles. Liebigs Ann. Chem., 397-399.

Ayrıntılar

Birincil Dil

İngilizce

Konular

Kimya Mühendisliği

Bölüm

Araştırma Makalesi

Yayımlanma Tarihi

1 Mart 2022

Gönderilme Tarihi

3 Ağustos 2021

Kabul Tarihi

11 Ekim 2021

Yayımlandığı Sayı

Yıl 2022 Cilt: 12 Sayı: 1

Kaynak Göster

APA
Arıkan Ölmez, N. (2022). Microwave-Assisted Synthesis of Acyclic Imides. Journal of the Institute of Science and Technology, 12(1), 317-323. https://doi.org/10.21597/jist.978327
AMA
1.Arıkan Ölmez N. Microwave-Assisted Synthesis of Acyclic Imides. Iğdır Üniv. Fen Bil Enst. Der. 2022;12(1):317-323. doi:10.21597/jist.978327
Chicago
Arıkan Ölmez, Nevin. 2022. “Microwave-Assisted Synthesis of Acyclic Imides”. Journal of the Institute of Science and Technology 12 (1): 317-23. https://doi.org/10.21597/jist.978327.
EndNote
Arıkan Ölmez N (01 Mart 2022) Microwave-Assisted Synthesis of Acyclic Imides. Journal of the Institute of Science and Technology 12 1 317–323.
IEEE
[1]N. Arıkan Ölmez, “Microwave-Assisted Synthesis of Acyclic Imides”, Iğdır Üniv. Fen Bil Enst. Der., c. 12, sy 1, ss. 317–323, Mar. 2022, doi: 10.21597/jist.978327.
ISNAD
Arıkan Ölmez, Nevin. “Microwave-Assisted Synthesis of Acyclic Imides”. Journal of the Institute of Science and Technology 12/1 (01 Mart 2022): 317-323. https://doi.org/10.21597/jist.978327.
JAMA
1.Arıkan Ölmez N. Microwave-Assisted Synthesis of Acyclic Imides. Iğdır Üniv. Fen Bil Enst. Der. 2022;12:317–323.
MLA
Arıkan Ölmez, Nevin. “Microwave-Assisted Synthesis of Acyclic Imides”. Journal of the Institute of Science and Technology, c. 12, sy 1, Mart 2022, ss. 317-23, doi:10.21597/jist.978327.
Vancouver
1.Nevin Arıkan Ölmez. Microwave-Assisted Synthesis of Acyclic Imides. Iğdır Üniv. Fen Bil Enst. Der. 01 Mart 2022;12(1):317-23. doi:10.21597/jist.978327

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