Step-economic, efficient, ZnS nanoparticle-catalyzed synthesis of spirooxindole derivatives in aqueous medium via Knoevenagel condensation followed by Michael addition
Silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (SB-DBU)Cl as a highly efficient, heterogeneous and recyclable silica-supported ionic liquid catalyst for the synthesis of benzo[b]pyran, bis(benzo[b]pyran) and spiro-pyran derivatives
The reaction of 3-chloropropyl silica (SilprCl) with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) in dry acetone affords silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (SB-DBU)Cl as a new silica-supported ionicliquid catalyst. Afterward, (SB-DBU)Cl is used for the efficientsynthesis of 4H-benzo[b]pyran derivatives via the one-pot, three-componentreaction of carbonyl compounds (cyclohexane-1
3-氯丙基二氧化硅(SilprCl)与1,8-二氮杂双环[5.4.0]十一碳-7-烯(DBU)在干燥的丙酮中的反应得到二氧化硅键合的5-正丙基-八氢-嘧啶基[1,2- a]氯化ze嗪(SB-DBU)Cl作为新型的二氧化硅负载型离子液体催化剂。之后,(SB-DBU)Cl通过羰基化合物(环己烷-1,3-二酮,5,5-一锅法)的三锅法有效合成4 H-苯并[ b ]吡喃衍生物。(1,3-二甲基环己烷-1,3-二酮或3-甲基-1-苯基-2-吡唑啉-5-酮)与芳族醛和烷基丙二酸酯。此外,一些新颖的双(苯并[ b使用(SB-DBU)Cl合成[] pyran] s和在结构上含有羟吲哚和/或喹喔啉部分的多种结构多样的螺-吡喃。将催化剂循环使用十五次,收率不变。
NaCl as a Novel and Green Catalyst for the Synthesis of Biodynamic Spiro Heterocycles in Water Under Sonication
Abstract An efficient and novel green catalytic protocol for the synthesis of biologically important spirooxindole derivatives is developed in a one-pot, three-componentapproach involving substituted isatin, activated methylene reagent, and 3-methyl-1-phenyl-2-pyrazolin-5-one in water under sonication. This report describes the use of sodium chloride as a nonacidic and green catalyst for a variety
Step-economic, efficient, ZnS nanoparticle-catalyzed synthesis of spirooxindole derivatives in aqueous medium via Knoevenagel condensation followed by Michael addition
作者:Anshu Dandia、Vijay Parewa、Anuj Kumar Jain、Kuldeep S. Rathore
DOI:10.1039/c1gc15244k
日期:——
An environmentally friendly, one-pot, three-component ZnS nanoparticle-mediated synthesis of biologically important spirooxindole derivatives in water under ultrasonic irradiation is described herein. ZnS nanoparticles were synthesized by aqueous chemical method. The advantages of this method lies in its simplicity, cost effectiveness, environment friendliness, easier scaling up for large scale synthesis without using high pressure, temperature and toxic chemicals. Greenness of the process was well instituted as water was exploited both as reaction media as well as medium for synthesis of catalyst (ZnS nanoparticles). The particle size was determined by transmission electron microscopy (TEM) and XRD. Compared with other methods for synthesis of spirooxindole derivatives, satisfactory results were obtained with high yields, short reaction time, with simple experimental procedure. After reaction course, the ZnS NPs can be recycled and reused without any apparent loss of activity.