Adding a certain compound to certain chemical reactions, such as: 5922-60-1, name is 2-Amino-5-chlorobenzonitrile, belongs to nitriles-buliding-blocks compound, 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 5922-60-1, Quality Control of 2-Amino-5-chlorobenzonitrile
1) Synthesis of (2-amino-5-chlorophenyl)cyclopropyl) methanone 2-Amino-5-chlorobenzonitrile (500 mg, 3.28 mmol) was dissolved in THF (10 mL), and while stirring the reaction solution at 0°C, cyclopropyl magnesium bromide (0.5 M THF solution, 26.4 mL) was added dropwise thereto. The reaction solution was stirred overnight under heating at 80°C, followed by ice-cooling, and 2 N hydrochloric acid was added thereto under ice-cooling. After the reaction solution was stirred at room temperature for 2 hours, the solution was diluted with ethyl acetate and then neutralized with a saturated aqueous sodium hydrogen carbonate solution. The organic layer was separated and washed with saturated brine and then dried over magnesium sulfate. After the drying agent was removed by filtration, the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane = 3/1), whereby (2-amino-5-chlorophenyl) (cyclopropyl) methanone (453 mg, 83percent) was obtained as a yellow solid. 1H-NMR (400 MHz, CDCl3) delta: 0.98-1.03 (2H, m), 1.16-1.20 (2H, m), 2.54-2.60 (1H, m), 6.61 (1H, d, J = 8.8 Hz), 7.21 (1H, dd, J = 8.8, 2.4 Hz), 7.92 (1H, d, J = 2.4 Hz)
At the same time, in my other blogs, there are other synthetic methods of this type of compound, 2-Amino-5-chlorobenzonitrile, and friends who are interested can also refer to it.
Reference:
Patent; Banyu Pharmaceutical Co., Ltd.; EP2210880; (2010); A1;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts