C3-Alkylation of Furfural Derivatives by Continuous Flow Homogeneous Catalysis

10 February 2023, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The C3-functionalization of furfural using homogeneous ruthenium catalysts requires the pre-installation of an ortho-directing imine group, as well as high temperatures, which did not allow scaling up, at least under batch conditions. In order to design a safer process, we set out to develop a continuous flow process specifically for the C3-alkylation of furfural (Murai reaction). The transposition of a batch process to a continuous flow process is often costly in terms of time and reagents. Therefore, we chose to proceed in two steps: the reaction conditions were first optimized using a laboratory-built pulsed-flow system to save reagents. The optimized conditions in this pulsed-flow mode were then successfully transferred to a continuous flow reactor. In addition, the versatility of this continuous flow device allowed both steps of the reaction to be carried out, namely the formation of the imine directing group and the C3-functionalization with some vinylsilanes and norbonene.

Keywords

Biomass
Furfural
C–H Activation
Homogeneous Catalysis
Flow

Supplementary materials

Title
Description
Actions
Title
Supporting information
Description
General Information, Characterization data, copies of NMR spectra
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.