Analyzing the synthesis route of 591-12-8

In addition to the literature in the link below, there is a lot of literature about this compound(5-Methylfuran-2(3H)-one)Synthetic Route of C5H6O2, illustrating the importance and wide applicability of this compound(591-12-8).

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 591-12-8, is researched, Molecular C5H6O2, about Transfer Hydrogenation of Methyl and Ethyl Levulinate Promoted by a ZrO2 Catalyst: Comparison of Batch vs. Continuous Gas-Flow Conditions, the main research direction is transfer hydrogenation methyl ethyl levulinate Zirconia catalyst.Synthetic Route of C5H6O2.

The catalytic conversion of Me and Et levulinates into γ-valerolactone (GVL) by using methanol, ethanol, and 2-propanol as the H-donor/solvent, promoted by the ZrO2 catalyst, is described as carried out under both batch and gas-flow conditions. Under batch conditions, 2-propanol was found to be the best H-donor mol., with Et levulinate giving the highest yield in GVL. The reactions occurring under continuous gas-flow conditions were found to be much more efficient, also showing excellent yields in GVL when EtOH was used as the reducing agent. These experiments clearly show that the ability to release hydrogen from the alc. H-donor/solvent is the main factor driving CTH processes, while the tendency to attack the esteric group is the key step in the formation of transesterification products.

In addition to the literature in the link below, there is a lot of literature about this compound(5-Methylfuran-2(3H)-one)Synthetic Route of C5H6O2, illustrating the importance and wide applicability of this compound(591-12-8).

Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia