Simple exploration of 5-(Hydroxymethyl)oxazolidin-2-one

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 7517-99-9

Reference of 7517-99-9, 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.7517-99-9, Name is 5-(Hydroxymethyl)oxazolidin-2-one, molecular formula is C4H7NO3. In a article，once mentioned of 7517-99-9

CuI/N,N-dimethylglycine catalyzed coupling of aryl bromides with substituted oxazolidinones took place at 120 C in DMF, affording the corresponding N-arylation products with good to excellent yields. A number of functional groups, such as ketone, nitrile, nitro, methoxy, and hydroxyl were tolerated under these conditions, thereby allowing diversity synthesis of N-aryloxazolidinones.

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 7517-99-9

Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H1307NO – PubChem