Synthetic Route of 497-25-6, 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.497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a article，once mentioned of 497-25-6
A series of chiral C2-symmetric compounds was prepared from readily available alpha,omega-diacyl chlorides and optically pure 2-oxazolidinone derivatives.Following preparation of the asymmetrically pure bis-oxazolidinone derivatives (6a-d, 11, 13, and 20), we prepared the dienolate of these compounds and quenched the reaction mixture with electrophiles such as iodomethane, allyl iodide, and benzyl bromide.Compounds 14a-e, and 15 were isolated with diastereomer ratios in excess of 9.8:1.If the chain length between the two carbonyl atoms was sufficiently small, dialkylation did not occur, but instead, provided cyclization products 18, 19, and 21.Mono-alkylated products 22a-c were prepared from 6c or 6d in modest yield.Unsymmetrical dialkylated compound 23 was prepared in 50percent yield from 22b.
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 497-25-6
Reference：
Oxazolidine – Wikipedia,
Oxazolidine | C3H1073NO – PubChem