Next Article in Journal
Synthesis of N-(N’-benzoylhydrazinomethyl)benzamide
Previous Article in Journal
2-(Pyrazin-2-yliminomethyl)phenol
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molbank
Volume 2007
Issue 2
10.3390/M524
molbank-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

2-[(2-Hydroxy-naphthalen-1-ylmethylene)-amino]- 5,6-dihydro-4H-cyclopenta [b] thiophene-3-carboxylic Acid Methyl Ester

by
Abdullah Mohamed Asiri
Chemistry Department, Faculty of Science, King Abdul-Aziz University, Jeddah 21413, P.O. Box 9028, Saudi Arabia
Molbank 2007, 2007(2), M524; https://doi.org/10.3390/M524
Submission received: 3 January 2006 / Accepted: 24 June 2006 / Published: 31 May 2007
Versions Notes

Schiff bases from 2-hydroxy-1-naphthaldehyde have often been used as chelating ligands in the field coordination chemistry [1]. The Schiff base compounds can be classified by their photochromic and thermochromic characteristics [2].
Molbank 2007 m524 i001
A solution of 2-Amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic acid methyl ester 1 (5.0g, 0.025mol) and 2-hydroxynaphthaldehyde 2 (4.3g, 0.025 mol) in absolute ethanol (100 mL) was heated under reflux for 5 hrs. Cooling the mixture, filtering the precipitate and recrystallization from ethanol gave the Schiff base 3 as red crystals (6.4g, 72.88%).
Melting Point: 208-210°C (EtOH).
IR (KBr; cm-1): 1701.2 (C=O), 1560.6 (C=N), 1453.4 (C=C), 1308.4 (C-O) and 1046.2 (C-N).
¹H NMR (400 MHz; CDCl3) δ, ppm: 14.93 (s, 1H, OH), 9.44 (s, 1H,=CH), 8.20- 7.27 (m, 6H, CHaromatic 6Haromatic), 3.99 (s, 3H,COOMe), 3.03-2.85 (t, 4H, 2 CH2), 2.46-2.22 (m, 2H, CH2).
¹³C NMR (100 MHz; CDCl3) δ, ppm: 27.50, 28.81, 29.78, 30.72, 49.69, 51.14, 54.05, 109.93, 118.92, 120.44, 123.17, 124.79, 127.40, 128.83, 130.32, 136.64, 146.45, 153.55, 158.86, 164.71.

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3

References

  1. Garnovski, A.D.; Nivorozhkin, A.L.; Minkin, V.I. Coord. Chem. Rev. 1993, 126, 1.
  2. Hadjoudis, E.; Vittorakis, M.; Maustakali-Mavridis, I. Tetrahedron 1987, 43, 1345.

Share and Cite

MDPI and ACS Style

Asiri, A.M. 2-[(2-Hydroxy-naphthalen-1-ylmethylene)-amino]- 5,6-dihydro-4H-cyclopenta [b] thiophene-3-carboxylic Acid Methyl Ester. Molbank 2007, 2007, M524. https://doi.org/10.3390/M524

AMA Style

Asiri AM. 2-[(2-Hydroxy-naphthalen-1-ylmethylene)-amino]- 5,6-dihydro-4H-cyclopenta [b] thiophene-3-carboxylic Acid Methyl Ester. Molbank. 2007; 2007(2):M524. https://doi.org/10.3390/M524

Chicago/Turabian Style

Asiri, Abdullah Mohamed. 2007. "2-[(2-Hydroxy-naphthalen-1-ylmethylene)-amino]- 5,6-dihydro-4H-cyclopenta [b] thiophene-3-carboxylic Acid Methyl Ester" Molbank 2007, no. 2: M524. https://doi.org/10.3390/M524

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop