Electric Literature 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
Mesoporous aluminium doped MCM-41 silica catalysts were prepared by a sol-gel method in two reaction steps (acid and alkaline hydrolysis) from joint hydrolysis of tetraethylortosilicate (TEOS) and aluminium triisoproxide, using n-dodecylammonium chloride as surfactant, at room temperature, and subsequent calcination at 550 C. Two solids with different Si/Al molar ratios (5 and 10) were synthesized, which possess high specific surface area and acidity, with both Broensted and Lewis acid sites. By using a biphasic water/MIBK as reaction medium and a 30 wt.% of the 10Al-MCM catalyst with respect to the substrate weight (glucose), 87% of glucose conversion and 36% of HMF yield were achieved at 195 C after 150 min of reaction time. The reaction is quite selective toward HMF, since only fructose was detected as by-product, but neither levulinic acid nor furfural were found. Moreover, the use of a sodium chloride aqueous solution (20 wt.%) and MIBK ameliorates the partition coefficient between the organic and the aqueous phases up to 1.9, leading to an enhancement of the glucose conversion and HMF yield, attaining values of 98% and 63%, respectively, in a time as short as 30 min. The catalytic performance of this acid solid, associated to the presence of strong acid sites, is well maintained after three catalytic cycles.
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