| Literature DB >> 31765514 |
Jeroen Bomon1, Elias Van Den Broeck2, Mathias Bal1, Yuhe Liao3, Sergey Sergeyev1, Veronique Van Speybroeck2, Bert F Sels3, Bert U W Maes1.
Abstract
An efficient conversion of biorenewable ferulic acid into bio-catechol has been developed. The transformation comprises two consecutive defunctionalizations of the substrate, that is, C-O (demethylation) and C-C (de-2-carboxyvinylation) bond cleavage, occurring in one step. The process only requires heating of ferulic acid with HCl (or H2 SO4 ) as catalyst in pressurized hot water (250 °C, 50 bar N2 ). The versatility is shown on a variety of other (biorenewable) substrates yielding up to 84 % di- (catechol, resorcinol, hydroquinone) and trihydroxybenzenes (pyrogallol, hydroxyquinol), in most cases just requiring simple extraction as work-up.Entities:
Keywords: C-dealkylation; O-dealkylation; bond cleavage; green chemistry; renewable resources
Year: 2020 PMID: 31765514 DOI: 10.1002/anie.201913023
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336