دورية أكاديمية

Multifunctional Biomass-Based Ionic Liquids/CuCl-Catalyzed CO2-Promoted Hydration of Propargylic Alcohols: A Green Synthesis of α-Hydroxy Ketones

التفاصيل البيبلوغرافية
العنوان: Multifunctional Biomass-Based Ionic Liquids/CuCl-Catalyzed CO2-Promoted Hydration of Propargylic Alcohols: A Green Synthesis of α-Hydroxy Ketones
المؤلفون: Ye Yuan, Siqi Zhang, Kang Duan, Yong Xu, Kaixuan Guo, Cheng Chen, Somboon Chaemchuen, Dongfeng Cao, Francis Verpoort
المصدر: International Journal of Molecular Sciences, Vol 25, Iss 3, p 1937 (2024)
بيانات النشر: MDPI AG, 2024.
سنة النشر: 2024
المجموعة: LCC:Biology (General)
LCC:Chemistry
مصطلحات موضوعية: ionic liquid, CO2, biomass, catalysis, α-hydroxy ketones, Biology (General), QH301-705.5, Chemistry, QD1-999
الوصف: α-Hydroxy ketones are a class of vital organic skeletons that generally exist in a variety of natural products and high-value chemicals. However, the traditional synthetic route for their production involves toxic Hg salts and corrosive H2SO4 as catalysts, resulting in harsh conditions and the undesired side reaction of Meyer–Schuster rearrangement. In this study, CO2-promoted hydration of propargylic alcohols was achieved for the synthesis of various α-hydroxy ketones. Notably, this process was catalyzed using an environmentally friendly and cost-effective biomass-based ionic liquids/CuCl system, which effectively eliminated the side reaction. The ionic liquids utilized in this system are derived from natural biomass materials, which exhibited recyclability and catalytic activity under 1 bar of CO2 pressure without volatile organic solvents or additives. Evaluation of the green metrics revealed the superiority of this CuCl/ionic liquid system in terms of environmental sustainability. Further mechanistic investigation attributed the excellent performance to the ionic liquid component, which exhibited multifunctionality in activating substrates, CO2 and the Cu component.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 25031937
1422-0067
1661-6596
Relation: https://www.mdpi.com/1422-0067/25/3/1937; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067
DOI: 10.3390/ijms25031937
URL الوصول: https://doaj.org/article/30f138b878714998a00880460d19c123
رقم الأكسشن: edsdoj.30f138b878714998a00880460d19c123
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:25031937
14220067
16616596
DOI:10.3390/ijms25031937