Synthetic Route of 56100-22-2, 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. 56100-22-2, Name is 6-Methyl-2,2′-bipyridine, molecular formula is C11H10N2. In a Article，once mentioned of 56100-22-2
One step nickel-catalyzed electroreductive homocoupling among 2-bromopicolines and 2-bromopyridine has been investigated by our group in an undivided cell and using zinc or iron as sacrificial anode. In this work, it was developed mono and dihalopyridines coupling to obtain possible products from heterocoupling. A series of reactions were carried out in order to develop a synthetic method for the preparation of unsymmetrical 2,2?-bipyridines and 2,2?:6?,2?-terpyridines. Statistical yields (50%) were observed for 2-bromopyridines/2-bromo-6-methylpyridine heterocoupling. In a preliminary study devoted to terpyridines preparation, good results were obtained for 2,6-dihalopyridines homocoupling, affording 2,6-dichloro-2, 2?-bipyridine (46%) and 2,6-dibromo-2,2?-bipyridine (56%), at controlled reaction time. At major reaction time, it was observed that the direct electroreduction of the 2,6?-dihalo-2,2?-bipyridines intermediates and 2,6?-dihalo-2,2?:6?,2?-terpyridines products on the cathode surface. A reasonable isolated product yield of 6,6?-dimethyl-2,2?:6?,2?-terpyridine (10%) was only observed in the reaction between 2,6-dichloropyridine and 2-bromo-6- methylpyridine (1:2).
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Synthetic Route of 56100-22-2, you can also check out more blogs about56100-22-2
Reference：
Metal catalyst and ligand design,
Ligand Template Strategies for Catalyst Encapsulation – NCBI