LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition
Transesterification is one of the important organic reactions employed in numerous industrial as well as laboratory applications for the synthesis of various esters. Herein, we report a rapid, highly efficient, and transition metal-free transesterification reaction in the presence of LiHMDS under so...
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doaj-2ea2f3458dd84446a26f3c7d1534ecc92021-03-19T07:03:25ZengElsevierCatalysis Communications1873-39052021-01-01149106194LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free conditionLavanya L. Mittapelli0Kiran R. Gore1Department of Chemistry, University of Mumbai, Mumbai 400098, IndiaDepartment of Chemistry, University of Mumbai, Mumbai 400098, India; Department of Chemistry, Indian Institute of Technology Kharagpur, West Bengal 721302, India; Corresponding author at: Department of Chemistry, Indian Institute of Technology Kharagpur, West Bengal-721302, India.Transesterification is one of the important organic reactions employed in numerous industrial as well as laboratory applications for the synthesis of various esters. Herein, we report a rapid, highly efficient, and transition metal-free transesterification reaction in the presence of LiHMDS under solvent-free conditions. The transesterification reaction was carried out with three different benzoate esters and a wide range of primary and secondary alcohols (from C3-C18) in good to excellent yields (45 examples). By considering the commercial role of esters, this method will be promising for the facile synthesis of esters in industry-relevant applications.http://www.sciencedirect.com/science/article/pii/S1566736720302703TransesterificationTransition metal-freeSolvent-freeLiHMDSBenzoate ester |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lavanya L. Mittapelli Kiran R. Gore |
spellingShingle |
Lavanya L. Mittapelli Kiran R. Gore LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition Catalysis Communications Transesterification Transition metal-free Solvent-free LiHMDS Benzoate ester |
author_facet |
Lavanya L. Mittapelli Kiran R. Gore |
author_sort |
Lavanya L. Mittapelli |
title |
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition |
title_short |
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition |
title_full |
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition |
title_fullStr |
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition |
title_full_unstemmed |
LiHMDS: Facile, highly efficient and metal-free transesterification under solvent-free condition |
title_sort |
lihmds: facile, highly efficient and metal-free transesterification under solvent-free condition |
publisher |
Elsevier |
series |
Catalysis Communications |
issn |
1873-3905 |
publishDate |
2021-01-01 |
description |
Transesterification is one of the important organic reactions employed in numerous industrial as well as laboratory applications for the synthesis of various esters. Herein, we report a rapid, highly efficient, and transition metal-free transesterification reaction in the presence of LiHMDS under solvent-free conditions. The transesterification reaction was carried out with three different benzoate esters and a wide range of primary and secondary alcohols (from C3-C18) in good to excellent yields (45 examples). By considering the commercial role of esters, this method will be promising for the facile synthesis of esters in industry-relevant applications. |
topic |
Transesterification Transition metal-free Solvent-free LiHMDS Benzoate ester |
url |
http://www.sciencedirect.com/science/article/pii/S1566736720302703 |
work_keys_str_mv |
AT lavanyalmittapelli lihmdsfacilehighlyefficientandmetalfreetransesterificationundersolventfreecondition AT kiranrgore lihmdsfacilehighlyefficientandmetalfreetransesterificationundersolventfreecondition |
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1724214582944202752 |