Academic Journal

One-Pot Synthesis of Push–Pull Butadienes from 1,3-Diethyl-2-thiobarbituric Acid and Propargylic Alcohols

التفاصيل البيبلوغرافية
العنوان: One-Pot Synthesis of Push–Pull Butadienes from 1,3-Diethyl-2-thiobarbituric Acid and Propargylic Alcohols
المؤلفون: Javier Francos, Victorio Cadierno
المصدر: Molbank, Vol 2022, Iss 3, p M1393 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Inorganic chemistry
مصطلحات موضوعية: push–pull molecules, butadienes, indium chloride, propargylic alcohols, Meyer–Schuster rearrangement, Knoevenagel condensation, Inorganic chemistry, QD146-197
الوصف: A new synthetic procedure for obtaining two previously reported donor-acceptor butadiene dyes, namely 5-(3,3-bis(4-methoxyphenyl)allylidene)-1,3-diethyl-2-thioxodihydropyrimidine-4,6(1H,5H)-dione and 5-(3,3-bis(4-(dimethylamino)phenyl)allylidene)-1,3-diethyl-2-thioxodihydropyrimidine-4,6(1H,5H)-dione, based on the InCl3-catalyzed coupling 1,3-diethyl-2-thiobarbituric acid with 1,1-bis(4-methoxyphenyl)prop-2-yn-1-ol and 1,1-bis(4-(dimethylamino)phenyl)prop-2-yn-1-ol, respectively, is presented. The reactions, which cleanly proceed in water under MW irradiation, involve the initial generation of the corresponding enals by Meyer-Schuster rearrangement of the alkynols and their subsequent Knoevenagel condensation with the 2-thiobarbituric acid derivative. By following the same approach, the novel butadiene 5-(3,3-bi([1,1′-biphenyl]-4-yl)allylidene)-1,3-diethyl-2-thioxodihydropyrimidine-4,6(1H,5H)-dione, which was characterized by 1H and 13C{1H} NMR, IR, UV-Vis, elemental analysis and HRMS, was synthesized in 79% yield.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1422-8599
Relation: https://www.mdpi.com/1422-8599/2022/3/M1393; https://doaj.org/toc/1422-8599
DOI: 10.3390/M1393
URL الوصول: https://doaj.org/article/bcfd137fabf84ac0a8359fd6af7581eb
رقم الانضمام: edsdoj.bcfd137fabf84ac0a8359fd6af7581eb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14228599
DOI:10.3390/M1393