3-Aminopropyltriethoxysilyl functionalized Na-Al-MCM-41 solid base catalyst for selective preparation of 2-phenylpropionitrile from phenylacetonitrile
Title | 3-Aminopropyltriethoxysilyl functionalized Na-Al-MCM-41 solid base catalyst for selective preparation of 2-phenylpropionitrile from phenylacetonitrile |
Publication Type | Journal Article |
Year of Publication | 2005 |
Authors | Venkatesan, C, Chidambaram, M, Singh, AP |
Journal | Applied Catalysis A-General |
Volume | 292 |
Pagination | 344-353 |
Date Published | SEP |
Type of Article | Article |
ISSN | 0926-860X |
Keywords | 2-phenylpropionitrile, base catalysis, dimethylcarbonate, monomethylation, NH2-Na-Al-MCM-41, phenylacetonitrile |
Abstract | Various solid base catalysts have been prepared by ion exchange of zeolites and Na-Al-MCM-41 and by organosilane grafting over mesoporous materials. Base catalysts thus synthesized were studied in the selective monomethylation of phenylacetonitrile (PAN) to 2-phenylpropionitrile (2-PPN) using dimethylcarbonate (DMC) as an alkylating agent in a Parr autoclave at a temperature ranging between 443 and 473 K and at autogenously developed pressure. NH2-Na-Al-MCM-41 (30) showed a high activity, and the optimum loading of 3-aminopropyltriethoxysilyl (3-APTES) was found to be 1.35 mmol g(-1), being consistent with the structural characterization. Co-condensation of 3-APTES, tetraethylorthosilicate (TEOS) and sodiumaluminate in the presence of surfactant provides a material with uniformly distributed basic sites responsible for high activity in the selective monomethylation of phenylacetonitrile. (c) 2005 Elsevier B.V. All rights reserved. |
DOI | 10.1016/j.apcata.2005.06.013 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 4.012 |