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Decarboxylative trifluoromethylthiolation of pyridylacetates.


ABSTRACT: Decarboxylative trifluoromethylthiolation of lithium pyridylacetates was achieved using N-(trifluoromethylthio)benzenesulfonimide as the electrophilic trifluoromethylthiolation reagent. The reaction afforded the corresponding trifluoromethyl thioethers in good yield. Furthermore, the preparation of lithium pyridylacetates by saponification of the corresponding methyl esters and subsequent decarboxylative trifluoromethylthiolation were performed in a one-pot fashion.

SUBMITTER: Kawanishi R 

PROVIDER: S-EPMC7849234 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

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Decarboxylative trifluoromethylthiolation of pyridylacetates.

Kawanishi Ryouta R   Nakada Kosuke K   Shibatomi Kazutaka K  

Beilstein journal of organic chemistry 20210125


Decarboxylative trifluoromethylthiolation of lithium pyridylacetates was achieved using <i>N</i>-(trifluoromethylthio)benzenesulfonimide as the electrophilic trifluoromethylthiolation reagent. The reaction afforded the corresponding trifluoromethyl thioethers in good yield. Furthermore, the preparation of lithium pyridylacetates by saponification of the corresponding methyl esters and subsequent decarboxylative trifluoromethylthiolation were performed in a one-pot fashion. ...[more]

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