Adding a certain compound to certain chemical reactions, such as: 218632-01-0, name is 3-Fluoro-4-nitrobenzonitrile, 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 218632-01-0, 218632-01-0
3- r(2R.3RJS)-7-Methyl-2.3-diDhenyl-14-dioxasDiror4.5ldec-7-yllmethyl amino)-4- nitrobenzonitrileA solution of acetonitrile (2049 ml.) in a 3 L flask was heated to 40 C. Next, potassium carbonate (198 g, 1434 mmol), 1-[(2R,3R,7S)-7-methyl-2,3-diphenyl-1 ,4- dioxaspiro[4.5]dec-7- yl]methanamine (242 g, 717 mmol) and 3-fluoro-4-nitrobenzonitrile (1 19 g, 717 mmol) were added slowly. The mixture was allowed to stir at 40 C for 2 h, and then cooled to RT. Stirring was continued at RT overnight. The next day, the slurry was filtered and the solids were washed with acetonitrile (500 ml_). The filtrate was concentrated to afford the crude product (while keeping the temperature -60 C during concentration). To the thick dark residue was added MeOH. The solution was heated to 60 C on the rotovap and concentrated to a minimal volume. To the residue was added -500 ml. of MeOH slowly with heating to avoid rapid crystallization, and the solution was heated to reflux. Once at reflux, an additional 250 ml. MeOH was slowly added. The resulting slurry was allowed to stir at reflux for about 60 min, then heating was stopped and the slurry was allowed to cool to RT and stirring was continued for 3 days. The slurry was cooled to -10 C with an ice/water bath. Stirring was continued for -2 h, and then the slurry was filtered and washed with cold MeOH (100 ml_). The solids were dried under reduced pressure to give the desired product as a bright orange solid (245 g, 70.7% yield). This material was used in the next step.
In the field of chemistry, the synthetic routes of compounds are constantly being developed and updated. I will also mention this compound in other articles, 3-Fluoro-4-nitrobenzonitrile, other downstream synthetic routes, hurry up and to see.
Reference:
Patent; GLAXOSMITHKLINE LLC; BROOKS, Carl; CHEUNG, Mui; EIDAM, Hilary, Schenck; GOODMAN, Krista, B.; HAMMOND, Marlys; HILFIKER, Mark, A.; HOANG, Tram, H.; PATTERSON, Jaclyn, R.; STOY, Patrick; YE, Guosen; WO2013/12500; (2013); A1;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts