Study of in situ generation of carbocationic system from trityl chloride (Ph3CCl) which efficiently catalyzed cross-aldol condensation reaction |
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Authors: | Abdolkarim Zare Maria Merajoddin Alireza Hasaninejad Ahmad Reza Moosavi-Zare Vahid Khakyzadeh |
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Institution: | 1. Department of Chemistry, Payame Noor University, PO BOX 19395-3697, Tehran, Iran;2. Department of Chemistry, Faculty of Sciences, Persian Gulf University, 75169 Bushehr, Iran;3. Department of Chemistry, University of Sayyed Jamaleddin Asadabadi, 6541835583 Asadabad, Iran;4. Faculty of Chemistry, Bu-Ali Sina University, 6517838683 Hamedan, Iran |
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Abstract: | Organocatalyst trityl chloride (Ph3CCl), by in situ formation of trityl carbocation with inherent instability, efficiently promotes the cross-aldol condensation reaction between cycloalkanones and arylaldehydes in solvent-free and homogeneous media to afford α,α′-bis(arylidene)cycloalkanones in high yields. Moreover, an attractive and plausible mechanism based on observations and the literature is proposed for the reaction. |
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