Solvent-free biginelli reactions catalyzed by hierarchical zeolite utilizing a ball mill technique: A green sustainable process

60Citations
Citations of this article
54Readers
Mendeley users who have this article in their library.

Abstract

sustainable, green one-pot process for the synthesis of dihydropyrimidinones (DHPMs) derivatives by a three-component reaction of β-ketoester derivatives, aldehyde and urea or thiourea over the alkali-treated H-ZSM-5 zeolite under ball-milling was developed. Isolation of the product with ethyl acetate shadowed by vanishing of solvent was applied. The hierachical zeolite catalyst (MFI27_6) showed high yield (86%-96%) of DHPMs in a very short time (10-30 min). The recyclability of the catalyst for the subsequent reactions was examined in four subsequent runs. The catalyst was shown to be robust without a detectable reduction in catalytic activity, and high yields of products showed the efficient protocol of the Biginelli reactions.

Cite

CITATION STYLE

APA

Shahid, A., Ahmed, N. S., Saleh, T. S., Al-Thabaiti, S. A., Basahel, S. N., Schwieger, W., & Mokhtar, M. (2017). Solvent-free biginelli reactions catalyzed by hierarchical zeolite utilizing a ball mill technique: A green sustainable process. Catalysts, 7(3). https://doi.org/10.3390/catal7030084

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free