108-48-5, Adding a certain compound to certain chemical reactions, such as: 108-48-5, 2,6-Dimethylpyridine, 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, 108-48-5, blongs to pyridine-derivatives compound.
In a separate flask, a mixture of 2,6-bis(methyl)pyridine(3.5 mL, 30 mmol) and N-bromosuccinimide (NBS) (10.70 g, 60.12 mmol) in CCl4 (400mL) was refluxed in the presence of azodiisobutyronitrile (AIBN) (0.15 g, 0.9 mmol) for 6 h under theirritation of 200 W lamp. After being cooled to room temperature, the mixture was filtered and the filtrate was concentrated in vacuo. Purification was achieved by flashed column chromatography using ethyl acetate / petroleum ether = 1 / 10 as eluent. The second band solution was collected, combined and evaporated in vacuo to afford the product as a white crystal (4.5 g, 37%). 1H NMR (delta, ppm,400 M, CDCl3): 4.55(s, CH2), 7.38 (d, Py, J= 7.76 Hz), 7.72 (q, Py).
These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,108-48-5, its application will become more common.
Reference:
Article; You, Xiuli; Wei, Zhenhong; Inorganica Chimica Acta; vol. 423; PA; (2014); p. 332 – 339;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem