A new application about (Tetrahydrofuran-3-yl)methanol

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 15833-61-1

Synthetic Route of 15833-61-1, 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.15833-61-1, Name is (Tetrahydrofuran-3-yl)methanol, molecular formula is C5H10O2. In a article，once mentioned of 15833-61-1

The Rh-ReOx/SiO2 (Re/Rh = 0.5) exhibited high activity in the hydrogenolysis of ethers with an OH group. The CO bond neighboring CH2OH group was selectively dissociated: The hydrogenolysis of tetrahydro-5-methyl-2-furfuryl alcohol and 2-isopropoxyethannol gave 1,5-hexanediol and ethanol + isopropanol, respectively. This tendency suggests the regioselective CO dissociation mechanism via anion intermediate formed by the attack of hydride and the subsequent protonation of the anion.

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 15833-61-1

Reference：
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem