Issue 7, 2019

Cooperation between an alcoholic proton and boryl species in the catalytic gem-hydrodiborylation of carboxylic esters to access 1,1-diborylalkanes

Abstract

Cooperation between an alcoholic proton and boryl species in the selective gem-hydrodiborylation of carboxylic esters is described. The simple iron salt FeBr2 was used as an effective catalyst. Experimental evidence suggests that the ester is initially hydrogenated with the alcoholic proton as the hydride source to provide an intermediate aldehyde, followed by a gem-diborylation with B2pin2 (bis(pinacolato)diboron) to selectively achieve gem-hydrodiborylation. The structure of the alkoxide used is important for chemoselective transformation of the ester functional group. When tert-butoxide is used, protonation of the iron boryl species to form an iron hydride species is rate-limiting, making hydrodiborylation of the ester selectively occur. When ethoxide or methoxide is used, the protonation of the iron boryl species to form an iron hydride species is relatively facile, making hydrogenation of the ester to an alcohol selectively occur with the alcoholic proton acting as the hydride source. With NaOtBu as the base and EtOH as the proton source, various aliphatic esters like ethyl acetate were selectively converted to 1,1-diborylalkanes in the presence of B2pin2. Diverse transformations of the obtained 1,1-diborylalkanes exhibit the advantages of this methodology for hetero multi-functionalization of ester functional groups for the synthesis of various value-added molecules.

Graphical abstract: Cooperation between an alcoholic proton and boryl species in the catalytic gem-hydrodiborylation of carboxylic esters to access 1,1-diborylalkanes

Supplementary files

Article information

Article type
Research Article
Submitted
27 ربيع الثاني 1440
Accepted
26 جمادى الأولى 1440
First published
27 جمادى الأولى 1440

Org. Chem. Front., 2019,6, 900-907

Cooperation between an alcoholic proton and boryl species in the catalytic gem-hydrodiborylation of carboxylic esters to access 1,1-diborylalkanes

Z. He, Q. Zhu, X. Hu, L. Wang, C. Xia and C. Liu, Org. Chem. Front., 2019, 6, 900 DOI: 10.1039/C9QO00007K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements