Introduction of a new synthetic route about 10380-28-6

The chemical industry reduces the impact on the environment during synthesis,10380-28-6,Bis(8-quinolinolato)copper(II),I believe this compound will play a more active role in future production and life.

10380-28-6, In the next few decades, the world population will flourish. As the population grows rapidly and people all over the world use more and more resources, all industries must consider their environmental impact. Bis(8-quinolinolato)copper(II), cas is 10380-28-6,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

General procedure: To a mixture of K3PO4 (18.8 g, 88.7 mmol), CuII oxinate (780 mg,2.22 mmol), KI (3.68 g, 22.2 mmol) and 2 (10.0 g, 22.2 mmol), water(30 mL) and acetonitrile (30 mL) were added. The mixture was stirredat 120 C for 3 days. Then brine was added, and the mixture was extracted with EA. The combined organic layers were dried with anhydrous MgSO4 and concentrated under reduced pressure. The residue was purified on a silica gel column with PE:DCM (3:1) as eluent to give3 (3.27 g, 51%) as a white solid. 1H NMR (400 MHz, CDCl3): delta (ppm)7.53 (d, J=8.8 Hz, 1H), 7.39 (d, J=8.0 Hz, 1H), 7.29 (t, J=8.4 Hz,1H), 7.11 (d, J=8.0 Hz, 1H), 7.03 (s, 1H), 6.98 (t, J=7.4 Hz, 1H),6.88 (d, J=8.0 Hz, 1H), 6.34 (d, J=7.2 Hz, 1H), 6.23 (d, J=7.6 Hz,1H). 13C NMR (125 MHz, CDCl3): delta (ppm) 161.1, 160.1, 131.7, 130.5,127.7, 126.7, 125.0, 124.5, 124.0, 121.5, 114.6, 111.0, 87.7, 85.8.Anal. Calcd for C14H9BrO2 (%): C, 58.16; H, 3.14; Br, 27.64; O, 11.07;Found: C, 58.03; H, 3.02; O, 10.98.

The chemical industry reduces the impact on the environment during synthesis,10380-28-6,Bis(8-quinolinolato)copper(II),I believe this compound will play a more active role in future production and life.

Reference£º
Article; He, Keqiang; Li, Weili; Tian, Hongkun; Zhang, Jidong; Yan, Donghang; Geng, Yanhou; Wang, Fosong; Organic electronics; vol. 57; (2018); p. 359 – 366;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

Introduction of a new synthetic route about 10380-28-6

With the rapid development of chemical substances, we look forward to future research findings about 10380-28-6

Bis(8-quinolinolato)copper(II), cas is 10380-28-6, it is a common heterocyclic compound, the copper-catalyst compound, its synthesis route is as follows.

General procedure: To a mixture of K3PO4 (18.8 g, 88.7 mmol), CuII oxinate (780 mg,2.22 mmol), KI (3.68 g, 22.2 mmol) and 2 (10.0 g, 22.2 mmol), water(30 mL) and acetonitrile (30 mL) were added. The mixture was stirredat 120 C for 3 days. Then brine was added, and the mixture was extracted with EA. The combined organic layers were dried with anhydrous MgSO4 and concentrated under reduced pressure. The residue was purified on a silica gel column with PE:DCM (3:1) as eluent to give3 (3.27 g, 51%) as a white solid. 1H NMR (400 MHz, CDCl3): delta (ppm)7.53 (d, J=8.8 Hz, 1H), 7.39 (d, J=8.0 Hz, 1H), 7.29 (t, J=8.4 Hz,1H), 7.11 (d, J=8.0 Hz, 1H), 7.03 (s, 1H), 6.98 (t, J=7.4 Hz, 1H),6.88 (d, J=8.0 Hz, 1H), 6.34 (d, J=7.2 Hz, 1H), 6.23 (d, J=7.6 Hz,1H). 13C NMR (125 MHz, CDCl3): delta (ppm) 161.1, 160.1, 131.7, 130.5,127.7, 126.7, 125.0, 124.5, 124.0, 121.5, 114.6, 111.0, 87.7, 85.8.Anal. Calcd for C14H9BrO2 (%): C, 58.16; H, 3.14; Br, 27.64; O, 11.07;Found: C, 58.03; H, 3.02; O, 10.98.

With the rapid development of chemical substances, we look forward to future research findings about 10380-28-6

Reference£º
Article; He, Keqiang; Li, Weili; Tian, Hongkun; Zhang, Jidong; Yan, Donghang; Geng, Yanhou; Wang, Fosong; Organic electronics; vol. 57; (2018); p. 359 – 366;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

 

New learning discoveries about 10380-28-6

The synthetic route of 10380-28-6 has been constantly updated, and we look forward to future research findings.

10380-28-6, Bis(8-quinolinolato)copper(II) is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: To a mixture of K3PO4 (18.8 g, 88.7 mmol), CuII oxinate (780 mg,2.22 mmol), KI (3.68 g, 22.2 mmol) and 2 (10.0 g, 22.2 mmol), water(30 mL) and acetonitrile (30 mL) were added. The mixture was stirredat 120 C for 3 days. Then brine was added, and the mixture was extracted with EA. The combined organic layers were dried with anhydrous MgSO4 and concentrated under reduced pressure. The residue was purified on a silica gel column with PE:DCM (3:1) as eluent to give3 (3.27 g, 51%) as a white solid. 1H NMR (400 MHz, CDCl3): delta (ppm)7.53 (d, J=8.8 Hz, 1H), 7.39 (d, J=8.0 Hz, 1H), 7.29 (t, J=8.4 Hz,1H), 7.11 (d, J=8.0 Hz, 1H), 7.03 (s, 1H), 6.98 (t, J=7.4 Hz, 1H),6.88 (d, J=8.0 Hz, 1H), 6.34 (d, J=7.2 Hz, 1H), 6.23 (d, J=7.6 Hz,1H). 13C NMR (125 MHz, CDCl3): delta (ppm) 161.1, 160.1, 131.7, 130.5,127.7, 126.7, 125.0, 124.5, 124.0, 121.5, 114.6, 111.0, 87.7, 85.8.Anal. Calcd for C14H9BrO2 (%): C, 58.16; H, 3.14; Br, 27.64; O, 11.07;Found: C, 58.03; H, 3.02; O, 10.98.

The synthetic route of 10380-28-6 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; He, Keqiang; Li, Weili; Tian, Hongkun; Zhang, Jidong; Yan, Donghang; Geng, Yanhou; Wang, Fosong; Organic electronics; vol. 57; (2018); p. 359 – 366;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”