Analyzing the synthesis route of 288-36-8

Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms.In my other articles, you can also check out more blogs about 1H-1,2,3-Triazole.

Electric Literature of 288-36-8, New Advances in Chemical Research in 2021. As an important bridge between the micro and macro material world, chemistry is one of the main methods and means for humans to understand and transform the material world. 288-36-8, name is 1H-1,2,3-Triazole, molecular formula is C2H3N3, its traditional synthetic route has been very mature, but the traditional synthetic route has various shortcomings, below Introduce a new synthetic route.

To a mixture of 2-bromo-4-fluorobenzoic acid (30 g, 137 mmol) , cesium carbonate (89.26 g, 274 mmol) , and CuI (5.27 g, 27.4 mmol) in DMF (200 mL) was added N, N? -dimethylcyclohexane-1, 2-diamine (3.7 mL, 23.3 mmol) and 1H-1, 2, 3-triazole (18.92 g, 274 mmol) . The resulting mixture was stirred at 110 overnight, cooled, concentrated in vacuo, and diluted with water (150 mL) . The aqueous layer was washed with EtOAc (300 mL x 3) . The aqueous layer was acidified with 2 N HCl and extracted with EtOAc (300 mL x 4) . The combined organic layers were washed with brine (150 mL x 3) , dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (petroleum ether: EtOAc100: 15: 1) to provide the title compound as a solid. LRMS m/z (M+H) 208.0 found, 208.0 required.

Therefore, this conceptually novel strategy might open impressive avenues to establish green and sustainable chemistry platforms.In my other articles, you can also check out more blogs about 1H-1,2,3-Triazole.

Reference:
Patent; MERCK SHARP & DOHME CORP.; KUDUK, Scott D.; LIVERTON, Nigel; LUO, Yunfu; (59 pag.)WO2016/101118; (2016); A1;,
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics