Adding a certain compound to certain chemical reactions, such as: 89-00-9, Pyridine-2,3-dicarboxylic acid, can increase the reaction rate and produce products with better performance than those obtained under traditional synthetic methods. Here is a downstream synthesis route of the compound, Safety of Pyridine-2,3-dicarboxylic acid, blongs to pyridine-derivatives compound. Safety of Pyridine-2,3-dicarboxylic acid
Synthesis of complex III was similar to that of II except that BaCl2 (0.105 g, 0.5 mmol) was used instead of FeCl2*4H2O (0.1268 g, 1 mmol). The pH was adjusted into 6, the mixture keep under autogenous pressure in 120C for 78 h, and then slowly cooled to room temperature at a rate of 5C/h. Then white crystals suitable for X-ray diffraction were separated and washed with water, which were stable in air and insoluble in water and common white solvents. The yield was 58% based on Ba.
At the same time, in my other blogs, there are other synthetic methods of this type of compound,89-00-9, Pyridine-2,3-dicarboxylic acid, and friends who are interested can also refer to it.
Reference:
Article; Huang; Shi; Liu; Xiao; Yin; Russian Journal of Coordination Chemistry; vol. 41; 5; (2015); p. 325 – 333; Koord. Khim.; vol. 41; 5; (2015); p. 325 – 333,9;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem