Synthetic Route of 497-25-6, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a Article，once mentioned of 497-25-6
We describe the synthesis and radical polymerization of series of styrenes with 2-oxazolidone moieties inherited from alpha-amino acids on the side chain. The 2-oxazolidone 2 was readily synthesized through the reaction of diphenyl carbonate with amino alcohols 1 that were prepared through the reduction of the corresponding alpha-amino acids (glycine, l-alanine, l-phenylalanine, l-valine, and l-methionine), in the presence of 1,8-diazabicyclo[5.4.0]-7-undecene as a base catalyst. The subsequent N-substitution reaction of 2-oxazolidone with 4-(chloromethyl) styrene in the presence of sodium hydride produced high yield of the corresponding styrenic compounds 3. Free radical polymerization of these monomers 3 smoothly proceeded in the quantitative monomer-conversion using benzoyl peroxide as a radical initiator to give the corresponding polymers (P3). The thermal properties of the resulting polymers were evaluated by differential scanning calorimetry and thermogravimetric analysis. These oxazolidone-containing polymers effectively adsorbed phenols from aqueous solution, and were also miscible with poly(4-vinylphenol) in the equimolar ratio mixture, because of the effective hydrogen bond interaction involving a carboxyl group of oxazolidone moieties and a hydroxyl group of the phenol.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 497-25-6. In my other articles, you can also check out more blogs about 497-25-6
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H1163NO – PubChem