Issue 24, 2016

Development of 6-amyl-α-pyrone as a potential biomass-derived platform molecule

Abstract

Catalytic transformation routes for the valorization of biomass-derived 6-amyl-α-pyrone (6PP) were explored for the first time. Ring-opening and decarboxylation of 6PP in water yielded non-2-en-4-one with 95% conversion and nearly 60% selectivity at 498 K, without the requirement of an acid catalyst. The decarboxylated product was further hydrogenated to yield 4-nonanone over a Pd/C catalyst. In order to produce longer chain hydrocarbons of diesel and jet fuel range, C–C coupling via aldol condensation of nonanone with furfural and 5-hydroxymethyl furfural (HMF) was experimented over a mixed oxide (CaO–MgO) catalyst measuring up to 40% and 60% yield of the branched aldol products at 443 K and 393 K respectively.

Graphical abstract: Development of 6-amyl-α-pyrone as a potential biomass-derived platform molecule

Supplementary files

Article information

Article type
Communication
Submitted
12 Sep 2016
Accepted
18 Oct 2016
First published
19 Oct 2016
This article is Open Access
Creative Commons BY license

Green Chem., 2016,18, 6431-6435

Development of 6-amyl-α-pyrone as a potential biomass-derived platform molecule

Md. I. Alam, S. Gupta, A. Bohre, E. Ahmad, T. S. Khan, B. Saha and M. A. Haider, Green Chem., 2016, 18, 6431 DOI: 10.1039/C6GC02528E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements