Palladium-Catalyzed Thiocarbonylations with Triisopropylsilyl Thioethers

Abstract

We have developed a palladium-catalyzed thiocarbonylation through the reaction of a σ-alkyl palladium intermediate with carbon monoxide and a triisopropylsilyl (TIPS) thioether. The use of CsF, (IPr)Pd(allyl)Cl [IPr =1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene], CO, and a TIPS thioether in THF are key to obtaining alkyl and aryl thioesters in high yields. The yield of the palladium-catalyzed thiocarbonylation depended on the structure of the substrate; indoline-2-one derivatives were formed faster than indoline derivatives. The reactions of benzoyl and hydrocinnamoyl fluorides with TIPSSPh and CsF also gave the corresponding thioesters.

Key words

palladium catalysis - thiocarbonylation - thioethers - thioesters - acyl fluorides

Publication History

Received: 20 November 2021

Accepted after revision: 07 January 2022

Accepted Manuscript online:
07 January 2022

Article published online:
02 February 2022

• References and Notes


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