Analyzing the synthesis route of 3544-25-0

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, 2-(4-Aminophenyl)acetonitrile, other downstream synthetic routes, hurry up and to see.

Adding a certain compound to certain chemical reactions, such as: 3544-25-0, name is 2-(4-Aminophenyl)acetonitrile, 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 3544-25-0, HPLC of Formula: C8H8N2

To a solution of 2-(4- m op^r^l) eton ^ (3D g, 22.70 mmol) i 40 mL dimemylformamide cooled with ice bathwas added N-bromosuccinimide (4.04 g, 22.70 mmol) in portions . The mixture was stirred at 0 for 30 minutes and then at a b ie t tenperature for 1 hour. Waterwas added. The precipitate was collected by filtranon, washed with water, and dried in a vacuum oven at 40 “C to give the title compound (35fjg, 16.9 mmol. 74.4 % yield).

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, 2-(4-Aminophenyl)acetonitrile, other downstream synthetic routes, hurry up and to see.

Reference:
Patent; ABBVIE INC.; ABBVIE PHARMACEUTICAL TRADING (SHANGHAI) CO., LTD.; FIDANZE, Steven D.; LIU, Dachun; MANTEI, Robert A.; MCDANIEL, Keith F.; PRATT, John; SHEPPARD, George S.; WANG, Le; BOGDAN, Andrew; HOLMS, James H.; DIETRICH, Justin D.; MARJANOVIC, Jasmina; HASVOLD, Lisa A.; DAI, Yujia; WO2014/139324; (2014); A1;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts