These common heterocyclic compound, 39786-34-0, name is Ethyl 2-(2-cyanophenoxy)acetate, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, such as complicated route, low yield, poor purity, etc, below Introduce a new synthetic route. Safety of Ethyl 2-(2-cyanophenoxy)acetate
To a 1000 mL flask 50.0 g (244 mmol) of the intermediate product (L-1) was added, stirred and 6.43 g (268 mmol) of sodium hydride in 500 ml of DMF (dimethylformamide) are added slowly at 0C. The reaction was allowed to proceed to room temperature for 10 hours. After confirming the completion of the reaction by TLC, 500 mL of dichloromethane and 2000 mL of distilled water were injected to separate the organic layer, and concentrated under reduced pressure to obtain 37.0 g (yield 64%) of intermediate L-2.
The synthetic route of Ethyl 2-(2-cyanophenoxy)acetate has been constantly updated, and we look forward to future research findings.
Reference:
Patent; CHEIL INDUSTRIES INC.; JEONG, SOO-YOUNG; YU, EUN-SUN; KANG, DONG-MIN; SHIN, JI-HUN; RYU, DONG-KYU; LEE, SANG-SHIN; LEE, HAN-IL; JANG, YU-NA; HAN, SU-JIN; HONG, JIN-SEOK; (35 pag.)KR2015/17817; (2015); A;,
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts