Marvi Omid, Fekri Leila Zare
Department of Chemistry, Payam Noor University, P.O. Box 19395-3697, Tehran, Iran.
Comb Chem High Throughput Screen. 2018;21(1):19-25. doi: 10.2174/1386207321666180102115733.
Citrus Juice as an efficient, cost-effective and green catalyst employed for one-pot synthesis of various β-substituted enaminones through the reaction of β- dicarbonyl compounds with different primary amines in a solvent-free conditions on silica gel as solid surface using grindstone technique in high yields and short reaction times. The presented procedure is operationally simple, practical and green.
The wide application of this procedure is demonstrated by the use of various substituted amines to react with β-dicarbonyl compounds. The method was successfully applied for primary amines (15 entries) and the related enaminones were well synthesized in good to excellent yields. Melting points were measured on an Electro thermal 9100 apparatus. 1HNMR and 13C NMR spectra were recorded on a FTNMR BRUKER DRX 500 Avence spectrometer. Chemical shifts were given in ppm from TMS as internal references and CDCl3 was used as the solvent as well. The IR spectra were recorded on a Perkin Elmer FT-IR GX instrument. The chemicals used in this work were purchased from Merck and Fluka chemical companies.
Grinding synthesis of citrus juice catalyzed enamination of 1,3-dicarbonyls (acetylacetone, methyl and ethyl-3-oxobutanoate) with various primary amines (aromatic and aliphatic) under solvent-free silica supported conditions was examined and studied (15 entries) and the obtained enaminones were well synthesized in good to excellent yields. Furthermore, the effect of various catalysts on the yield and reaction time for grinding synthesis of 3-phenylamino- but- 2- enoic acid ethyl ester (1) by this method has evaluated as well.
A novel, efficient and green protocol for the grinding synthesis of enaminones using citrus juice as natural catalyst has been presented. This methodology is user friendly, green and low cost procedure under mild reaction condition with faster reaction rates. The citrus juice is inexpensive and non-toxic which makes the process convenient, more economic and benign. Furthermore, applying grindstone technique in solvent-free conditions, use of silica gel as a solid and heterogeneous surface in reaction, high yields of products, cleaner reaction profiles, and availability of the reagents makes this method a better choice for synthetic chemists.
柑橘汁作为一种高效、经济且绿色的催化剂,用于在无溶剂条件下,以硅胶为固体表面,采用研磨技术,通过β - 二羰基化合物与不同伯胺反应一锅法合成各种β - 取代烯胺酮,反应产率高且反应时间短。所呈现的方法操作简单、实用且绿色环保。
通过使用各种取代胺与β - 二羰基化合物反应,证明了该方法的广泛应用。该方法成功应用于伯胺(15个实例),相关烯胺酮均以良好至优异的产率顺利合成。熔点在电热9100仪器上测定。1H NMR和13C NMR光谱在FTNMR布鲁克DRX 500 Avence光谱仪上记录。化学位移以相对于TMS的ppm给出作为内标,CDCl3也用作溶剂。红外光谱在珀金埃尔默FT - IR GX仪器上记录。本工作中使用的化学品购自默克和富凯化学公司。
研究了在无溶剂硅胶负载条件下,柑橘汁催化1,3 - 二羰基化合物(乙酰丙酮、甲基和乙基 - 3 - 氧代丁酸酯)与各种伯胺(芳香族和脂肪族)的研磨合成烯胺反应(15个实例),所得到的烯胺酮均以良好至优异的产率顺利合成。此外,还评估了各种催化剂对该方法研磨合成3 - 苯基氨基 - 丁 - 2 - 烯酸乙酯(1)的产率和反应时间的影响。
提出了一种使用柑橘汁作为天然催化剂研磨合成烯胺酮的新颖、高效且绿色的方案。该方法在温和的反应条件下,反应速率更快,对用户友好、绿色且成本低。柑橘汁价格低廉且无毒,使得该过程方便、更经济且环保。此外,在无溶剂条件下应用研磨技术,在反应中使用硅胶作为固体和非均相表面,产物产率高,反应过程更清洁,且试剂易得,使得该方法成为合成化学家的更好选择。