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A Novel and Simple Experimental Procedure for Synthesizing, Purifying, and Identifying Coumarin in Undergraduate Heterocyclic Chemistry Laboratories (Record no. 45346)

MARC details
000 -LEADER
fixed length control field 02836nam a22002057a 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20240117160826.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 240116b ||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
ISSN 0021-9584
100 ## - MAIN ENTRY--AUTHOR NAME
Personal name García-Aranda, Mónica I.
245 ## - TITLE STATEMENT
Title A Novel and Simple Experimental Procedure for Synthesizing, Purifying, and Identifying Coumarin in Undergraduate Heterocyclic Chemistry Laboratories
Remainder of title (Journal Article)
260 ## - PUBLICATION, DISTRIBUTION, ETC. (IMPRINT)
Place of publication Washington DC
Name of publisher : American Chemical Society
Year of publication , 2023
300 ## - PHYSICAL DESCRIPTION
Number of Pages 4001–4006p.
440 ## - SERIES STATEMENT/ADDED ENTRY--TITLE
Title Journal of Chemical Society
Volume number/sequential designation , Volume 100: Number 10, October 2023
505 ## - FORMATTED CONTENTS NOTE
Formatted contents note ***______{For Hard Copy, Please visit Library.}________***<br/><br/>
520 ## - SUMMARY, ETC.
Summary, etc Abstract: Heterocyclic compounds are an integral part of research, particularly in the pharmaceutical field. The synthesis of such compounds in an undergraduate laboratory can help students understand the relevance and importance of their field of study. Our experimental activity introduces a novel procedure to synthesize coumarin, a heterocyclic formed by two fused rings, using commercial reagents and equipment found in most undergraduate teaching laboratories. What sets our proposed procedure apart is its short reaction time (15 min), high yields (80–85%), and avoidance of extreme experimental conditions, making it highly suitable for implementation in heterocyclic chemistry laboratories at the undergraduate level. The reaction mechanism is straightforward and easily comprehensible to students. Additionally, the fluorescence properties of coumarin are utilized to visually inspect the reaction’s progress and the corresponding purification procedure, enhancing the experiment’s pedagogical value and piquing the student’s curiosity. We successfully implemented this experimental proposal in three different groups, involving approximately 90 students, and received enthusiastic feedback. The heterocyclic compound obtained in the laboratory was highly engaging for the students, as it allowed them to apply the theoretical knowledge gained in their classes to practical experiments. They had the opportunity to explore the reactivities of the functional groups and witness the formation of a compound of great biological importance. The synthesis of heterocycles with notable biological applications serves as an exciting activity for the students. The fluorescent properties of the formed coumarin not only identify the product by visual inspection but also allow them to delve into the concept of fluorescence.
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical Term Coumarin| Pharmaceutical Engineering Degree| Heterocyclic Chemistry| Heterocyclic Chemistry Laboratory| Apprenticeship| Identification Techniques| Thin Layer Chromatography
700 ## - ADDED ENTRY--PERSONAL NAME
Personal name Franco-Pérez, Marco | Zamudio-Medina, Angel
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier https://doi.org/10.1021/acs.jchemed.3c00272
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Periodicals
Holdings
Lost status Damaged status Home library Current library Date acquired Koha item type
    RIE BPL Library RIE BPL Library 17.01.2024 Periodicals

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