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Branched Diol Monomers from the Sequential Hydrogenation of Renewable Carboxylic Acids
Author(s) -
Spanjers Charles S.,
Schneiderman Deborah K.,
Wang Jay Z.,
Wang Jingyu,
Hillmyer Marc A.,
Zhang Kechun,
Dauenhauer Paul J.
Publication year - 2016
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201600710
Subject(s) - chemistry , monomer , diol , petrochemical , yield (engineering) , triol , lactone , selectivity , green chemistry , organic chemistry , polyester , catalysis , polymer , aqueous solution , reaction mechanism , materials science , metallurgy
A prominent challenge in replacing petrochemical polymers with bioderived alternatives is the efficient transformation of biomass into useful monomers. In this work, we demonstrate a practical process for the synthesis of multifunctional alcohols from five‐ and six‐carbon acids using heterogeneous catalysts in aqueous media. Design of this process was guided by thermodynamic calculations, which indicate the need for two sequential high‐pressure hydrogenations: one, reduction of the acid to a lactone at high temperature; two, further reduction of the lactone to the corresponding diol or triol at low temperature. For example, the conversion of mesaconic acid into (α or β)‐methyl‐γ‐butyrolactone was achieved with 95 % selectivity at a turnover frequency of 1.2 min −1 over Pd/C at 240 °C. Subsequent conversion of (α or β)‐methyl‐γ‐butyrolactone into 2‐methyl‐1,4‐butanediol was achieved with a yield of 80 % with Ru/C at 100 °C. This process is an efficient method for the production of lactones, diols, and triols, all valuable monomers for the synthesis of bioderived branched polyesters.