Application of 15804-19-0, 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.15804-19-0, Name is Quinoxaline-2,3(1H,4H)-dione, molecular formula is C8H6N2O2. In a article£¬once mentioned of 15804-19-0
A solvent-free one step conversion of ketones to amides via Beckmann rearrangement catalysed by FeCl3¡¤6H2O in presence of hydroxylamine hydrochloride
FeCl3¡¤6H2O catalyses the direct conversion of ketones to amides via Beckmann rearrangement in the presence of hydroxylamine hydrochloride in good to excellent yields. No additional organic solvent is required. This solid phase reaction involves in situ formation of oxime, cleavage of C-C bond and formation of C-N bond. FeCl3¡¤6H2O is inexpensive, stable, easy to handle and eco-friendly.
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 15804-19-0
Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N356 | ChemSpider