120083-60-5Relevant academic research and scientific papers
Selective decarboxylation: A facile synthesis of 3-pyridinecarboxylic acid derivative
Wang, Junhua,Wang, Honglin,Ren, Hongmin,Dong, Lihua
, p. 4139 - 4142 (2009)
A convenient synthesis of 5-trifluoromethyl-3-pyridinecarboxylic acid was developed, involving palladium-catalyzed carbonylation, hydrolysis, and decarboxylation. This novel route features inexpensive starting material and easy operations.
Preparation of dihydropyrrol derivatives as intermediates
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Page/Page column 4-5, (2009/06/27)
The invention is concerned with a new scalable process for the preparation of compounds of formula I comprising a new process for the preparation of the key intermediate, a dihydropyrrole derivative formula II or a salt thereof.
Synthetic process development and scale up of palladium-catalyzed alkoxycarbonylation of chloropyridines
Crettaz, Roger,Waser, Jerome,Bessard, Yves
, p. 572 - 574 (2013/09/07)
2,3-Dichloropyridines undergo a mono- or a dicarbonylation in the presence of carbon monoxide, an alcohol, and a palladium catalyst, affording selectively either alkyl 3-chloropyridine-2-carboxylates or dialkyl pyridine-2,3-dicarboxylates in good yields, depending on the reaction conditions. For instance, the process could be scaled up for the monoalkoxycarbonylation of 2,3-dichloro-5-(trifluoromethyl)pyridine, affording in high yield and selectivity the corresponding 3-chloro-5-(trifluoromethyl)pyridine-2-carboxylate.
