Reductive Hydroformylation of Isosorbide Diallyl Ether - Université d'Artois Access content directly
Journal Articles Molecules Year : 2021

Reductive Hydroformylation of Isosorbide Diallyl Ether

Abstract

Isosorbide and its functionalized derivatives have numerous applications as bio-sourced building blocks. In this context, the synthesis of diols from isosorbide diallyl ether by hydrohydroxymethylation reaction is of extreme interest. This hydrohydroxymethylation, which consists of carbon-carbon double bonds converting into primary alcohol functions, can be obtained by a hydroformylation reaction followed by a hydrogenation reaction. In this study, reductive hydroformylation was achieved using isosorbide diallyl ether as a substrate in a rhodium/amine catalytic system. The highest yield in bis-primary alcohols obtained was equal to 79%.
Fichier principal
Vignette du fichier
2021 10.3390-molecules26237322.pdf (2.92 Mo) Télécharger le fichier
Origin : Publisher files allowed on an open archive
Licence : CC BY - Attribution

Dates and versions

hal-03675976 , version 1 (15-11-2023)

Identifiers

Cite

Jérémy Ternel, Adrien Lopes, Mathieu Sauthier, Clothilde Buffe, Vincent Wiatz, et al.. Reductive Hydroformylation of Isosorbide Diallyl Ether. Molecules, 2021, 26 (23), pp.7322. ⟨10.3390/molecules26237322⟩. ⟨hal-03675976⟩
31 View
3 Download

Altmetric

Share

Gmail Facebook X LinkedIn More