Synthetic Route of 2144-40-3, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.2144-40-3, Name is (cis-Tetrahydrofuran-2,5-diyl)dimethanol, molecular formula is C6H12O3. In a article，once mentioned of 2144-40-3
Biomass into chemicals: Conversion of sugars to furan derivatives by catalytic processes
Recently, the production of furan derivatives from sugars has become exciting in chemistry and in catalysis studies, because it aids one of the major routes for achieving sustainable energy supply and chemicals production. 5-Hydroxymethylfurfural (5-HMF), 2,5-furan-dicarboxylic acid (2,5-FDCA) and 2,5-dimethylfuran (2,5-DMF) have been called the “sleeping giants” of renewable intermediate chemicals. 5-HMF is a dehydration product of hexoses and a potential substitute of petroleum-based building blocks of various polymers. 2,5-FDCA is derived from oxidative dehydration of hexoses and is considered as one of the top 12 compounds made from a sugar into a value-added chemical [T. Werpy, G. Petersen, Top Value Added Chemicals From Biomass, 2004. Available electronically at http://www.osti.gov/bridge]. 2,5-DMF is produced through hydrogenation of HMF and is less volatile and of 40% higher energy density than ethanol. This review discusses mainly the catalytic routes for the synthesis of 5-HMF, 2,5-FDCA, 2,5-DMF and other furanic derivatives from sugars. Meanwhile, the possible reaction mechanism for the conversion of hexoses is discussed, and furthermore, some promising research orientations and advantageous catalysts are suggested based on the major problems encountered in the recent research.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 2144-40-3
Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem