Academic Journal

Multistep Microwave-Assisted Synthesis of Avobenzone

التفاصيل البيبلوغرافية
العنوان: Multistep Microwave-Assisted Synthesis of Avobenzone
اللغة: English
المؤلفون: Jordan, Annalisa M., Wilke, Ashley E., Nguyen, Tanifa L., Capistrant, Katelyn C., Zarbock, Katie R., Batiste Simms, Morgan E., Winsor, Brandi R., Wollack, James W. (ORCID 0000-0003-3124-721X)
المصدر: Journal of Chemical Education. Mar 2022 99(3):1435-1440.
الاتاحة: Division of Chemical Education, Inc. and ACS Publications Division of the American Chemical Society. 1155 Sixteenth Street NW, Washington, DC 20036. Tel: 800-227-5558; Tel: 202-872-4600; e-mail: eic@jce.acs.org; Web site: http://pubs.acs.org/jchemeduc
Peer Reviewed: Y
Page Count: 6
تاريخ النشر: 2022
نوع الوثيقة: Journal Articles
Reports - Evaluative
Education Level: Higher Education
Postsecondary Education
Descriptors: Organic Chemistry, Science Instruction, Laboratory Experiments, Hands on Science, Radiation, College Science, Science Experiments
DOI: 10.1021/acs.jchemed.1c00818
تدمد: 0021-9584
مستخلص: Multistep synthesis is a key capstone experience in organic laboratory instruction. Here, a four-step synthesis of avobenzone, an active component in sunscreens, has been developed that can be completed in two 4 h laboratory periods. This synthesis incorporates green principles and includes an aldol condensation, electrophilic addition of bromine to an alkene, an E2 dehalogenation of a dibromide, and hydration of an alkyne. Highlights of this synthesis include the use of coupling constants to identify alkene configuration, NMR analysis to determine preferred tautomeric form, the use of microwave irradiation to reduce reaction times, a solvent-free synthesis of a chalcone, and a three-step reaction that can be completed in a single lab period.
Abstractor: As Provided
Entry Date: 2022
رقم الانضمام: EJ1328598
قاعدة البيانات: ERIC
الوصف
تدمد:0021-9584
DOI:10.1021/acs.jchemed.1c00818