Volume 11, Issue 3 (2-2011)
2011, 11(3): 117-124 |
Back to browse issues page
Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:
rahmani S. Using SnCl4/EtOH as a new, fast, inexpensive and efficient method for aldol condensation of aromatic aldehydes and cycloalkanones. Journal title 2011; 11 (3) :117-124
URL: http://jsci.khu.ac.ir/article-1-1431-en.html
URL: http://jsci.khu.ac.ir/article-1-1431-en.html
student of P.H.D of semnan university
Abstract: (5678 Views)
An efficient, mild and environmentally- friendly approach was developed for the synthesis of bis arylidine cycloalkanones. SnCl4 was found as efficient catalyst for cross aldol condensation of cycloalkanones and aromatic aldehyde for synthesis of &alpha,&alpha'-bis(substituted-benzylidine) cycloalkanones in ethanol as a green solvent. In this method, the reaction works easily for a variety of aldehydes with both electron-donating and electron-with-drawing groups to give corresponding &alpha,&alpha’-bis(substituted-benzylidene) cyclohexanones in good to excellent yields. Comparing the known methods, the main advantages of our method are short time, user-friendly, low cost procedure, clean and environmentally benign reagents with ease of separation of the product and mild reaction condition with good to excellent yield for products
Type of Study: Research Paper |
Published: 2011/02/15
Published: 2011/02/15
Send email to the article author
| Rights and permissions | |
 | This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |
