4359-51-7Relevant articles and documents
Conversion of 2,3-Butanediol over Phosphate Catalysts
Nikitina, Maria A.,Ivanova, Irina I.
, p. 1346 - 1353 (2016/04/20)
2,3-Butanediol (BDO) is an excellent feedstock for expanding the network of bio-based chemicals through catalytic technologies. The dehydration of BDO provides an alternative green route to important chemicals such as methyl ethyl ketone (MEK) and 1,3-butadiene (BD). In this contribution, we report on the catalytic performance of boron (BP), aluminum (AlP), titanium (TiP), zirconium (ZrP), and niobium (NbP) phosphates in BDO dehydration. The kinetic study points to three reaction pathways operating over phosphate catalysts, leading to MEK, 2-methyl-propanal (MP), and BD via intermediate 3-butene-2-ol (3B2OL) formation. The major reaction pathway is shown to involve pinacol rearrangement to MEK. The reactivity of phosphates is found to increase in the order: BPTiPZrP=NbPAlP. The best catalytic performance is achieved over AlP, which shows the highest selectivity towards MEK (78 %) at 100 % 2,3-butanediol conversion.
Transformation of 1,2-diols over perfluorinated resinsulfonic acids (Nafion-H)
Bucsi,Bucsi, Imre,Molnar,Molnar, Arpad,Bartok,Bartok, Mihaly,Olah,Olah, George A.
, p. 8195 - 8202 (2007/10/02)
The transformations of 1,2-diols over perfluorinated resinsulfonic acids (Nafion-H) were studied, and correlations were examined between the structures of the investigated diols, the possible dehydration routes and the catalytic properties of Nafion-H. Comparisons were also made between the catalytic properties of Nafion-H and NaHX zeolite. Because of its stronger acidity, Nafion-H functions at temperatures considerably lower than those for the usual dehydrating catalysts, e.g. the zeolites. As is well established for other solid electrophilic catalysts, the dehydration of 1,2-diols mainly proceeds via the pinacol rearrangement. The lower temperatures and the stronger acidity of Nafion-H strongly favour the pinacol rearrangement versus 1,2-elimination. The reaction conditions are also advantageous for the formation of substituted 1,3-dioxolanes in a secondary condensation step between the unreacted diol and the primarily formed carbonyl compounds. Nafion-H gradually deactivates during long use, but it can be partially reactivated by washing with acetone.