microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones
نویسندگان
چکیده
microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones by the crossed- aldol condensation reaction of substituted aryl aldehydes with ketones in the presence of catalytic amount of nbcl5 in good to excellent yields. this reaction is carried out under solvent-free conditions. the results showed that aldehydes bearing electron–donating substituent's on phenyl-ring favored the formation of product in good to excellent yields with reaction times ranging between 3 and 7 min. in addition, furfural, cinamaldehyde, thiophene-2-carbaldehyde and 5-methylthiophene-2-carbaldehyde were investigated in aldol reaction, and the results showed excellent yields. also, the reactions were carried out at room & thermal (80 0c) conditions. the results showed that the yields are in accordance with the microwave irradiations, but the time is 1.5-5 h at room temperature and 15-45 min in thermal conditions.
منابع مشابه
Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones
Microwave assisted green synthesis of α, ά- bis (substituted- benzylidene) alkanones by the crossed- aldol condensation reaction of substituted aryl aldehydes with ketones in the presence of catalytic amount of NbCl5 in good to excellent yields. This reaction is carried out under solvent-free conditions. The results showed that aldehydes bearing electron–donating substituent's on phenyl-ring fa...
متن کاملP-Dodecylbenzenesulfonic acid (DBSA), a Brønsted acidSurfactant Catalyst for Synthesis of α, ά-bis(substituted benzylidene)cycloalkanones with Electron-Withdrawing Substituent in Aqueous Media
An array of aromatic aldehydes with electron withdrawing groupunderwent crossed-Aldol condensation with cycloalkanone in the presence of catalytic amounts of DBSA under aqueous media to afford the corresponding α, ά-bis(substituted-benzylidene) cycloalkanones in good yields. The electronic effects on aromatic aldehydes could be observed. The present method is operationally simple and use of wat...
متن کاملA facile solvent free Claisen-Schmidt reaction: synthesis of α,α'-bis-(substituted-benzylidene)cycloalkanones and α,α'-bis-(substituted-alkylidene)cycloalkanones.
Solvent-free Claisen-Schmidt reactions of cycloalkanones with various substituted benzaldehydes (aryl aldehydes) using solid NaOH (20 mol%) and applying a grinding technique were studied. Quantitative yields (96-98%) of α,α'-bis-(substituted-benzylidene)cycloalkanones were obtained. Aliphatic aldehydes also provided α,α'-bis-(substituted-alkylidene)cycloalkanones in very good yields with minor ...
متن کاملAn efficient synthesis of α,α'-benzylidene bis(4-hydroxycoumarin) derivatives catalyzed by Tl2O3 nanoparticles
In this work, we attempted to synthesize thallium (III) oxide nano structures by direct thermal decomposition using thallium I phenylsuccinic acid coordination polymer [Tl(PsucH)]n as a precursor. Also, Tl2O3 nanoparticles have been characterized by scanning electron microscopy (SEM), X-Ray powder diffraction (XRD) and IR spectroscopy and then we report a simple and efficient method for the syn...
متن کاملAn efficient synthesis of α,α'-benzylidene bis(4-hydroxycoumarin) derivatives catalyzed by Tl2O3 nanoparticles
In this work, we attempted to synthesize thallium (III) oxide nano structures by direct thermal decomposition using thallium I phenylsuccinic acid coordination polymer [Tl(PsucH)]n as a precursor. Also, Tl2O3 nanoparticles have been characterized by scanning electron microscopy (SEM), X-Ray powder diffraction (XRD) and IR spectroscopy and then we report a simple and efficient method for the syn...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
iranian chemical communicationناشر: payame noor university (pnu)
ISSN 2423-4958
دوره 3
شماره Issue 2, pp. 85-179 2015
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023