Synthetic Route of 954239-61-3, 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.954239-61-3, Name is Methyl 5-bromobenzo[d]oxazole-2-carboxylate, molecular formula is C9H6BrNO3. In a article£¬once mentioned of 954239-61-3
Method for synthesizing aromatic heterocyclic methyl ester compounds (by machine translation)
The invention discloses a method for synthesizing aromatic heterocyclic methyl ester compounds, namely to the molecular formula is [(ArN=C (CH3 ) NCH2 CH2 NCH2 C6 H5 ) CH] of Cl imidazole chlorine salt (wherein Ar=2, 6 – II – CH (CH3 )2 – C6 H3 ) As catalyst, normal pressure through the aromatic heterocyclic compound and carbon dioxide of the carboxylation reaction to synthesize aromatic heterocyclic methyl ester compound. This is by the imidazole salt catalyzed by aromatic heterocyclic compound and carbon dioxide of the carboxylation reaction to prepare aromatic heterocyclic methyl ester compound of the 1st example, compared with the prior art, not only the catalyst more green, synthetic more easily, and the mild reaction conditions, with equal or better tolerability of catalytic activity and functional group. (by machine translation)
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 954239-61-3
Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem