نویسندگان | شیوا علیزاده,حسین نعیمی,محسن مرادیان |
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همایش | 2nd Iranian Student Chemistry Conference |
تاریخ برگزاری همایش | ۲۰۱۵-۱۰-۶ |
محل برگزاری همایش | رشت |
نوع ارائه | سخنرانی |
سطح همایش | ملی |
چکیده مقاله
The indole ring system is probably the most ubiquitous heterocycle that represents an important structural component in many pharmacologically active compounds, agrochemistry and materials science1 . Although many methods have been developed for the synthesis of indoles2 , compared with other methodologies for indole synthesis, the Fischer indole synthesis through the reaction of ketones with aryhydrazines remains an extremely useful and important method3 . Since its discovery in the 1880s by Emil Fischer, various catalysts have been used to effect the cyclization of enolizable N-arylhydrazones derived from ketones and arylhydrazones. As the catalysts for the Fischer indole synthesis, Bronsed acids (H2SO4, HCl, PPA, AcOH, and TsOH) 4 , Lewis acids (ZnCl2 and TiCl4) 5 , and solid acids (zeolite and montmorillonite clay) 6 , have been reported. The reported Br ّ nsted and Lewis acids are environmentally unfriendly, hazardous, difficult to reuse, and usually required large amounts. Modified magnetic nanoparticles with acidic ionic liquid (Fe3O4@SiO2@IL) have been used as a heterogeneous, recyclable, and efficient catalyst for synthesis of some indole derivatives in good yields under microwave irradiation. Ketone was mixed with Fe3O4@SiO2.TBAPS.SO3H in toluene, and phenylhydrazine was added. The mixture was then stirred at 120°C for about 15 min under microwave irradiation. Reaction progress was monitored by GC–MS. After completion, the reaction mixture was cooled to room temperature, the Fe3O4@SiO2@IL were removed by use of an external magnetic field. The solvent was evaporated under reduced pressure. The solid products obtained were collected by filtration (scheme 1).