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 in | Green chemistry : an international journal and green chemistry resource : GC Vol. 23; no. 7; pp. 2652 - 2657 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
CAMBRIDGE
Royal Soc Chemistry
13.04.2021
Royal Society of Chemistry |
Subjects | |
Online Access | Get full text |
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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. |
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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 |