Adding a certain compound to certain chemical reactions, such as: 102074-19-1, (5-Methylpyridin-3-yl)methanol, 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, Computed Properties of C7H9NO, blongs to pyridine-derivatives compound. Computed Properties of C7H9NO
Step 2. 5-methyl-3-pyridinecarboxaldehyde. A mixture of 5-methyl-3-pyridinemethanol (106 mg, 0.86 mmol) and activated MnO2 (376 mg) in methylenechloride (10 mL) was stirred at room temperature overnight. The black solid of MnO2 was removed by filtration. The filtrate was concentrated in vacuo to yield the title compound as an oil (100 mg, 85%). 1H NMR (CDCl3): 10.10 (s, 1H), 8.89 (s, 1H), 8.68 (s, 1H), 7.98 (s, 1H), 2.45 (s, 3H)
At the same time, in my other blogs, there are other synthetic methods of this type of compound,102074-19-1, (5-Methylpyridin-3-yl)methanol, and friends who are interested can also refer to it.
Reference:
Patent; Cytovia, Inc.; EP1230232; (2004); B1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem