Archives for Chemistry Experiments of 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 497-25-6

Reference of 497-25-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.497-25-6, Name is Oxazolidin-2-one, molecular formula is C3H5NO2. In a Article,once mentioned of 497-25-6

LiOtBu Promoted 5-Exo?dig Cyclization of Propargyl Alcohols and Isocyanates for the Synthesis of Multisubstituted 3H-Oxazol-2-ones and Oxazolidin-2-ones

This study presents an efficient procedure for synthesis of 3,4,5-trisubstituted 3H-oxazol-2-ones and 3,4-disubstituted (Z)-oxazolidin-2-ones from substituted propargyl alcohols and aryl/alkyl isocyanates in the presence of LiOtBu, a base, and DMF, a solvent. This one-step, low-cost and gram scale synthesis exhibits superior atom economy, good to excellent yields, enhanced substrate scope and, high functional group tolerance and uses column chromatography-free purifications. Further, a product containing bromo substituent was successfully examined for Suzuki coupling with a view to amplifying the complexity of the molecule. Finally, the three component (aniline, Di-tert-butyldicarbonate and propargyl alcohol) reaction was demonstrated to get the oxazolon-2-ones (3H-oxazol-2-one and 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 497-25-6

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H960NO – PubChem