Two-Step Synthesis of 4-Hydroxy-3,5-dimethylphenyl Benzoate: Undergraduate Organic Laboratory of Electrophilic Aromatic Substitution and Nucleophilic Aromatic Substitution
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Huifa Han [1] ; Yali Qin [1] ; Fan Wang [1] ; Ning Ding [1] ; Fang Fang [1] ; Lihong Hu [1] ; Hongming Jin [1] ; Yinan Zhang [1]
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[1] Nanjing University of Chinese Medicine
Nanjing University of Chinese Medicine
China
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- Localización: Journal of chemical education, ISSN 0021-9584, Vol. 101, Nº 6, 2024, págs. 2406-2412
- Idioma: inglés
- Texto completo no disponible (Saber más ...)
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Resumen
Electrophilic aromatic substitution (SEAr) and nucleophilic aromatic substitution (SNAr) reactions are among the most valuable reactions in the conversion of aromatic rings. While these reactions are typically covered in separate experiments in undergraduate organic courses, a continuous experimental setup elucidating both SEAr and SNAr processes remains unexplored in the literature for undergraduate laboratories. We herein described a two-step experimental design to cascade the SEAr and SNAr reactions, aiding students in better understanding the similarities and differences of these conversions as well as introducing the concept of umpolung. The experiment also reinforces students’ proficiency in fundamental organic synthesis techniques and workup procedures, such as TLC analysis, chromatography purification, recrystallization, and handling LRMS and NMR.
