Category: 54231-35-5

Simple exploration of 3-Fluoro-2-nitropyridine

At the same time, in my other blogs, there are other synthetic methods of this type of compound,54231-35-5, 3-Fluoro-2-nitropyridine, and friends who are interested can also refer to it.

Adding a certain compound to certain chemical reactions, such as: 54231-35-5, 3-Fluoro-2-nitropyridine, 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, Recommanded Product: 54231-35-5, blongs to pyridine-derivatives compound. Recommanded Product: 54231-35-5

Step 1: A mixture of 3-fluoro-2-nitropyridine (3 g, 21.1 mmol) and K2CO3 (5.8 g, mmol) in MeOH (30 mL) was refluxed for lh and then cooled to room temperature. The mixture was filtered and the filtrate evaporated to give crude 32-2 as a yellow oil. LC-MS: m/z = 155.1 [M+H]+.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,54231-35-5, 3-Fluoro-2-nitropyridine, and friends who are interested can also refer to it.

Reference:
Patent; BIOGEN IDEC MA INC.; HUTCHINGS, Richard, H.; JONES, John, Howard; CHAO, Jianhua; ENYEDY, Istvan, J.; MARCOTTE, Douglas; WO2014/28669; (2014); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Simple exploration of 3-Fluoro-2-nitropyridine

At the same time, in my other blogs, there are other synthetic methods of this type of compound,54231-35-5, 3-Fluoro-2-nitropyridine, and friends who are interested can also refer to it.

Adding a certain compound to certain chemical reactions, such as: 54231-35-5, 3-Fluoro-2-nitropyridine, 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, Recommanded Product: 54231-35-5, blongs to pyridine-derivatives compound. Recommanded Product: 54231-35-5

Step 1: A mixture of 3-fluoro-2-nitropyridine (3 g, 21.1 mmol) and K2CO3 (5.8 g, mmol) in MeOH (30 mL) was refluxed for lh and then cooled to room temperature. The mixture was filtered and the filtrate evaporated to give crude 32-2 as a yellow oil. LC-MS: m/z = 155.1 [M+H]+.

At the same time, in my other blogs, there are other synthetic methods of this type of compound,54231-35-5, 3-Fluoro-2-nitropyridine, and friends who are interested can also refer to it.

Reference:
Patent; BIOGEN IDEC MA INC.; HUTCHINGS, Richard, H.; JONES, John, Howard; CHAO, Jianhua; ENYEDY, Istvan, J.; MARCOTTE, Douglas; WO2014/28669; (2014); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem