Evidence map›Paper›PMID 38383516›Full record

ArticleBMC chemistry2024

Application of α-bromination reaction on acetophenone derivatives in experimental teaching: a chemical innovation experiment engaging junior undergraduates.

Yongguang Gao, Na Chen, Xiaoye Jiang, Xiaochun Yang

Abstract read
In one paragraph

Article in BMC chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yongguang GaoDepartment of Chemistry, Tangshan Normal University, Tangshan, China. gaoyongguang@nwpu.edu.cn.ORCID http://orcid.org/0000-0003-1754-3426
Na ChenDepartment of Chemistry, Tangshan Normal University, Tangshan, China.
Xiaoye JiangDepartment of Chemistry, Tangshan Normal University, Tangshan, China.
Xiaochun YangDepartment of Chemistry, Tangshan Normal University, Tangshan, China.

Funding

Education Reform Project of Hebei Province 2021GJJG555Key Cultivation Project of Tangshan Normal University ZDPY05Key Project for Scientific Research in Colleges and Universities of Hebei province ZD2021408Natural Science Foundation of Hebei Province 2021105001Scientific Research Foundation of Tangshan Normal University 2021A03
6 · The paper itself

Abstract

The α-bromination reaction of carbonyl compounds is a significant topic in the field of organic chemistry. However, due to the lack of suitable brominating reagents, the application of this reaction in undergraduate organic chemistry experiments is limited. In this study, three junior undergraduates successfully conducted an innovative experiment under the guidance of teachers. The bromination of various acetophenone derivatives was investigated by employing pyridine hydrobromide perbromide as the brominating agent, with a focus on exploring the effects of reaction time, reaction temperature, and dosage of the brominating agent. The results demonstrated that 4-chloro-α-bromo-acetophenone could be synthesized at 90 ℃ using 4-chloroacetophenone as a substrate and acetic acid as a solvent with a molar ratio of substrate to brominator being 1.0:1.1. Through the experimental teaching of 18 junior undergraduates, it was observed that all the students successfully completed the experiment within a time frame of 4-5 h, with a notable achievement yield exceeding 80% observed in 14 students. This innovative experiment exhibits significant advantages in terms of safety, high yield, cost-effectiveness, and repeatability. Furthermore, while reinforcing fundamental skills in chemistry experimentation among students, it enhances their scientific literacy levels and fosters innovation consciousness as well as practical aptitude. Consequently, this approach is highly suitable for widespread implementation and integration into undergraduate experimental pedagogy.

Indexed as

Acetic acidAcetophenoneExperimental pedagogyPyridine hydrobromide perbromideα-Substitution

Identifiers

PMID38383516
PMCPMC10882791

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