Next Article in Journal
2-Mercapto-5-(2'-isopropyl-5'-methylphenoxymethyl)-1,3,4-triazole
Previous Article in Journal
3-Cyano-2-(2,5-dimethoxybenzalamino)-4-5-tetramethylenethiophene
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 6
Issue 6
10.3390/M213
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Short Note

3-(2-Nitrophenyl)-2-(4-nitrophenyl)-4-thiazolidinone

by
Abdullah Mohamed Asiri
Chemistry Department, Faculty of Science, King Abdul-Aziz University, Jeddah 21589, P.O. Box 80203, Saudi Arabia
Molecules 2001, 6(6), M213; https://doi.org/10.3390/M213
Submission received: 18 December 2000 / Accepted: 15 May 2001 / Published: 25 May 2001
(This article belongs to the Section Molbank Section of Molecules, 1997-2001)
Versions Notes
Molecules 06 m213 i001
The 4-thiazolidinone 3 was prepared from the Schiff base 1 thioglycolic acid 2 [1,2]. A mixture of 4-(Nitrobenzalamino)-(2-nitrobenzen) 1 (3.0 g, 0.011 mmol) and thioglycolic acid 2 (1.02 g, 0.011 mol) was refluxed for 15 hours at 110-120 oC in an oil bath. Sodium bicarbonate solution was added for removal of excess thioglycolic acid. The product was isolated and recrystallized from ethanol as orange crystals (3.52 g, 92%).
Mp. 70-72 °C (EtOH, uncorrected).
UV lmax (nm; Acetone)/e (dm3.mol-1.cm-1) 280/3185, 401/6107.
IR (KBr) 1690 (C=O), 700 (C-S-C).
1H-NMR (400 MHz; CDCL3; Me4Si) dH3.09 (2H, CH2), 6.07 (1H, d, S-CH), 6.71 (2H, dd, J = 7.6 Hz), 6.81 (2H, d, J = 8.3 Hz), 7.36 (2H, d, J = 7.33 Hz), 8.11 (2H, d, J = 8.5 Hz).
13C NMR (100 MHz; CDCl3):: 20.0 (CH2), 51.8 (C-S), 111.83, 116.1, 116.97, 118.75, 126.22, 135.65, 144.65, 196.24.
Anal.Calc. for C15H11N3O5S (345.339): C 52.17, H 3.21, N 12.17; found : C 52.33, H 3.11 , N 11.98.

Supplementary Materials

References

  1. Patoli, V. N.; Patel, P. K.; Xi, A. J. J. Indian Chem. Soc. 1994, 71, 683.
  2. Ergenc, N.; Capan, G.; Guenay, N. S.; Oezkirimli, S.; Geuengoer, M.; Oezbey, S.; Kendi, E. Archi der Pharm. 1999, 332, 343. [CrossRef]
Sample availability: available from the authors and MDPI.

Share and Cite

MDPI and ACS Style

Asiri, A.M. 3-(2-Nitrophenyl)-2-(4-nitrophenyl)-4-thiazolidinone. Molecules 2001, 6, M213. https://doi.org/10.3390/M213

AMA Style

Asiri AM. 3-(2-Nitrophenyl)-2-(4-nitrophenyl)-4-thiazolidinone. Molecules. 2001; 6(6):M213. https://doi.org/10.3390/M213

Chicago/Turabian Style

Asiri, Abdullah Mohamed. 2001. "3-(2-Nitrophenyl)-2-(4-nitrophenyl)-4-thiazolidinone" Molecules 6, no. 6: M213. https://doi.org/10.3390/M213

APA Style

Asiri, A. M. (2001). 3-(2-Nitrophenyl)-2-(4-nitrophenyl)-4-thiazolidinone. Molecules, 6(6), M213. https://doi.org/10.3390/M213

Article Metrics

Back to TopTop