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One-pot synthesis of nitroalkenes via the Henry reaction over amino-functionalized MIL-101 catalysts

Paper ID Volume ID Publish Year Pages File Format Full-Text
49844 46769 2012 4 PDF Available
Title
One-pot synthesis of nitroalkenes via the Henry reaction over amino-functionalized MIL-101 catalysts
Abstract

Ethylenediamine moieties with different amounts were incorporated into the metal–organic framework MIL-101 to prepare the amino-functionalized MIL-101 materials, which were used as heterogeneous catalysts in the one-pot synthesis of nitroalkenes via the Henry reaction. Various reaction conditions were optimized. Under the optimized conditions, the selectivity towards nitroalkenes is extremely high in combination with nearly complete conversion of the reactant nitroalkanes. The amino-functionalized MIL-101 behaves as a true heterogeneous catalyst, can be easily recovered by filtration, and can be reused at least twice without significant loss of its catalytic performance.

Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Amino-functionalized MIL-101 catalyst was prepared and applied in the Henry reaction. ► One-pot synthesis of nitroalkenes via the Henry reaction over the catalysts ► High selectivity for nitroalkenes with nearly complete conversion of nitroalkanes ► The catalysts behave as a true heterogeneous catalyst and can be easily recovered.

Keywords
Nitroalkanes; CC bond formation; Henry reaction; Metal–organic frameworks
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One-pot synthesis of nitroalkenes via the Henry reaction over amino-functionalized MIL-101 catalysts
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Publisher
Database: Elsevier - ScienceDirect
Journal: Catalysis Communications - Volume 29, 5 December 2012, Pages 101–104
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Catalysis
Get Full-Text Now
Don't Miss Today's Special Offer
Price was $35.95
You save - $31
Price after discount Only $4.95
100% Money Back Guarantee
Full-text PDF Download
Online Support
Any Questions? feel free to contact us