Oxidative esterification of alcohols by a single-side organically decorated Anderson-type chrome-based catalyst

The direct esterification of alcohols with non-noble metal-based catalytic systems faces great challenges. Here, we report a new chrome-based catalyst stabilized by a single pentaerythritol decorated Anderson-type polyoxometalate, [N(C 4 H 9 ) 4 ] 3 [CrMo 6 O 18 (OH) 3 C{(OCH 2 ) 3 CH 2 OH}], which...

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Published inGreen chemistry : an international journal and green chemistry resource : GC Vol. 23; no. 7; pp. 2652 - 2657
Main Authors Wang, Jingjing, Jiang, Feng, Tao, Chaofu, Yu, Han, Ruhlmann, Laurent, Wei, Yongge
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 13.04.2021
Royal Society of Chemistry
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Summary:The direct esterification of alcohols with non-noble metal-based catalytic systems faces great challenges. Here, we report a new chrome-based catalyst stabilized by a single pentaerythritol decorated Anderson-type polyoxometalate, [N(C 4 H 9 ) 4 ] 3 [CrMo 6 O 18 (OH) 3 C{(OCH 2 ) 3 CH 2 OH}], which can realize the efficient transformation from alcohols to esters by H 2 O 2 oxidation in good yields and high selectivity without extra organic ligands. A variety of alcohols with different functionalities including some natural products and pharmaceutical intermediates are tolerated in this system. The chrome-based catalyst can be recycled several times and still keep the original configuration and catalytic activity. We also propose a reasonable catalytic mechanism and prove the potential for industrial applications. An efficient strategy was reported for oxidative esterification reaction by a single-side organic decorated Anderson-type chrome-based catalyst in high yield. The Cr III Mo 6 -OH could be simply recycled many times and maintain high catalytic activity.
Bibliography:Electronic supplementary information (ESI) available: Experimental conditions, ESI table and NMR spectra. See DOI
10.1039/d1gc00161b
ISSN:1463-9262
1463-9270
DOI:10.1039/d1gc00161b