New Advances in Chemical Research, May 2021. Synthetic Route of 2682-49-7, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. 2682-49-7, Name is Thiazolidin-2-one, molecular formula is C3H5NOS. In a Article，once mentioned of 2682-49-7
The reaction between polystyrene 3-formylsalicylate and 2-Aminobenzylalcohol in DMF in the presence of ethyl acetate results in the formation of polystyrene N-(2-hydroxymethylphenyl)-2′-hydroxybenzylideneimine-3′- carboxylate (I). A benzene suspension of I reacts with mercaptoacetic acid undergoes cyclization and forms polystyrene N-(2-hydroxymethylphenyl)-C-(3′-carboxy-2′-hydroxyphenyl)thiazolidine-4-one, PSCH2?LH2 (II). A DMF suspension of II reacts with Mn(II) and Cd(II) ions and forms the corresponding polystyrene-anchored coordination compounds, [PSCH2?LHMn(OAc)(DMF)3] (III) and [PSCH2?LHCd(OAc)(DMF)] (IV). The polystyrene-anchored coordination compounds have been characterized on the basis of elemental analyses, spectral (IR, reflectance) studies and magnetic susceptibility measurements. II behave as a monobasic bidentate OS donor ligand in the coordination compounds. An octahedral structure for III and tetrahedral structure for IV are suggested.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Synthetic Route of 2682-49-7, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 2682-49-7, in my other articles.
Reference：
Quinuclidine – Wikipedia,
Quinuclidine | C7H359N | ChemSpider