Tag: M.W:100-200

It is a common heterocyclic compound, the copper-catalyst compound, Copper(I) bromide, cas is 7787-70-4 its synthesis route is as follows.,7787-70-4

Triethyl phosphite (183g, 1.1 mol) was added to a suspension of copper(I) bromide (164.5 g, 1.15 mol) in toluene (500 ml). The mixture was heated at 80C for 3 h with stirring, then left to cool and settle. The clear solution was decanted from the solid residue and the solvent evaporated on a rotary evaporator at 60C, to provide copper(I) bromide triethyl phosphite complex as a clear colourless oil, 336g (94% crude yield).

With the complex challenges of chemical substances, we look forward to future research findings about Copper(I) bromide

Reference£º
Patent; ASTRAZENECA AB; ASTRAZENECA UK LIMITED; WO2006/67416; (2006); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Name is Copper(I) bromide, as a common heterocyclic compound, it belongs to copper-catalyst compound, and cas is 7787-70-4, its synthesis route is as follows.

A dry and Ar-flushed Schlenk flask was charged with P(OEt)3 (5.2 mL, 30.0 mmol) in benzene (30 mL). CuBr (4.3 g, 30.0 mmol) was added. After the mixture had stirred at r.t. for 1 h and at 80 C for 1 h, unsolved solid was removed by filtration under Ar atmosphere and solvents were evaporated from the filtrate. The resulted mixture was cooled down to -78 C and was washed with n-hexane (2*). The remained solid was dried under vacuum; this gave CuBr*P(OEt)3. Yield: 6.8 g (73%); a mixture of oil and solid.

7787-70-4, 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.,7787-70-4 ,Copper(I) bromide, other downstream synthetic routes, hurry up and to see

Reference£º
Article; Moriya, Kohei; Schwaerzer, Kuno; Karaghiosoff, Konstantin; Knochel, Paul; Synthesis; vol. 48; 19; (2016); p. 3141 – 3154;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

As a common heterocyclic compound, it belongs to copper-catalyst compound, name is Copper(I) bromide, and cas is 7787-70-4, its synthesis route is as follows.

General procedure: An acetonitrile solution (5 mL) of cuprous chloride (0.008 g,0.084 mmol) was introduced dropwise to a solution of 1(0.040 g, 0.084 mmol) in dichloromethane (5 mL). The reactionwas allowed to stir at room temperature for 6 h. Afterthat, solvent was evaporated under vacuum to give microcrystallineproduct of 5 as a white solid.

7787-70-4, 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.,7787-70-4 ,Copper(I) bromide, other downstream synthetic routes, hurry up and to see

Reference£º
Article; Kumar, Saurabh; Balakrishna, Maravanji S; Journal of Chemical Sciences; vol. 129; 8; (2017); p. 1115 – 1120;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, 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. Copper(I) bromide, cas is 7787-70-4,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

General procedure: In a round bottom flask, copper(I) halide (0.1mmol, CuBr for 1 or CuI for 2) was dissolved in 2mL of MeCN. Under continuous stirring, a 5mL MeCN:EtOH (3:2) solution of HC(3-PhPz)3 (0.11mmol, 50mg) was added dropwise. The produced light brown solution was stirred at room temperature for 3h, then its volume was reduced by evaporation to ca. 2mL. Hexane (10mL) was added and the obtained precipitate was filtered off, recrystallized from a mixture of CH2Cl2 and hexane (1:1) to afford complexes 1 or 2 as colourless crystals. [CuBr(TpmPh)] (1): Yield (45.9mg) 78%. Elemental analysis calcd (%) for C28H22BrCuN6¡¤CH2Cl2: C 51.92, H 3.61, N 12.53; found: C 51.51, H 3.70, N 12.64. FTIR (KBr): nu (cm-1)=1532m, 1491 w, 1442m, 1391 w, 1342 w, 1324 w, 1299 w, 1268 w, 1242m, 1209m, 1095m, 1077m, 1038m, 798m, 756s, 688s. Far IR (CsI): nu (cm-1)=221m nu(Cu-Br). 1H NMR (300MHz, DMSO-d6, delta): 9.10 (s, 1H, HC(3-PhPz)3), 8.11 (br, 3H, 5-H-pz), 7.85 (br, 6H, o-H-Ph), 7.42 (br, 9H, m,p-H-Ph), 6.95 (br, 3H, 4-H-pz). 13C{1H} NMR (300MHz, DMSO-d6, delta): 152.14 (3-C-pz), 132.20 (Cquat-Ph), 131.82 (5-C-pz)), 128.76 (m-C-Ph), 128.32 (p-C-Ph), 125.53 (o-C-Ph), 104.57 (4-C-pz), 82.09 (HC(3-Phpz)3). ESI(+)MS in MeCN (m/z assignment, % intensity): 546 ({[HC(3-Phpz)3]Cu+MeCN}+, 100), 505 ({[HC(3-Phpz)3]Cu}+, 23).

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Copper(I) bromide, 7787-70-4

Reference£º
Article; Mahmoud, Abdallah G.; Martins, Luisa M.D.R.S.; Guedes da Silva, M. Fatima C.; Pombeiro, Armando J.L.; Inorganica Chimica Acta; vol. 483; (2018); p. 371 – 378;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Copper(I) bromide, cas is 7787-70-4, it is a common heterocyclic compound, the copper-catalyst compound, its synthesis route is as follows.,7787-70-4

General procedure: 0.018g (0.182mmol) of CuCl was added to 0.340g (0.205mmol) of [PPh4]2[1] dissolved in 20mL of MeCN solution. After stirring the resultant solution for 1hat RT, the yellowish brown solution formed, which was filtered, and solvent was removed in vacuo. The precipitate was washed with Et2O and extracted with THF, then recrystallized with Et2O/MeOH/THF to give [PPh4]2[2a] (0.250g, 0.143mmol, 79% based on CuCl). Similarly, under the same reaction conditions, using CuBr and CuI, we have isolated a yellowish brown solid of [PPh4]2[2b] (96% based on CuBr) and [PPh4]2[2c] (71% based on CuI), respectively, upon crystallization from Et2O/THF.

With the rapid development of chemical substances, we look forward to future research findings about Copper(I) bromide

Reference£º
Article; Shieh, Minghuey; Miu, Chia-Yeh; Liu, Yu-Hsin; Chu, Yen-Yi; Hsing, Kai-Jieah; Chiu, Jung-I; Lee, Chung-Feng; Journal of Organometallic Chemistry; vol. 815-816; (2016); p. 74 – 83;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

It is a common heterocyclic compound, the copper-catalyst compound, Copper(I) bromide, cas is 7787-70-4 its synthesis route is as follows.,7787-70-4

A solution of CuBr (0.0173 g, 0.12 mmol) in 10 mL of acetonitrile was added dropwise to a solution of 4 (0.048 g, 0.12 mmol) in 10 mL of dichloromethane at room temperature. The reaction mixture was stirred for 4 h. The solvent was removed under reduced pressure to obtain 8 as a brown crystalline solid. Yield: 82% (0.054 g). Mp: >195 C (dec). Anal. Calc. for C42H44Cu2Br2N2P2Se2¡¤CH3CN: C, 46.99; H, 4.21; N, 3.74. Found: C, 46.77; H, 4.10; N, 3.79%. 1H NMR (400 MHz, CDCl3) delta 7.73-7.02 (m, Ar, 28H), 3.43 (s, CH2, 4H), 2.46 (s, NMe2, 12H). 31P{1H} NMR (162 MHz, CDCl3): delta 23.2 (br s).

With the complex challenges of chemical substances, we look forward to future research findings about Copper(I) bromide

Reference£º
Article; Ananthnag, Guddekoppa S.; Edukondalu, Namepalli; Mague, Joel T.; Balakrishna, Maravanji S.; Polyhedron; vol. 62; (2013); p. 203 – 207;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

It is a common heterocyclic compound, the copper-catalyst compound, Copper(I) bromide, cas is 7787-70-4 its synthesis route is as follows.

General procedure: 0.022g (0.222mmol) of CuCl was added to 0.180g (0.109mmol) of [PPh4]2[1] dissolved in 20mL of MeCN solution at -35C. After stirring the resultant solution for 5min, the yellowish brown solution formed, which was filtered, and the filtrate was concentrated. A solution of Et2O (60mL) was added into the filtrate to precipitate the product at -35C. The precipitate was then washed with Et2O and dried to give [PPh4]2[3a] (0.107g, 0.058mmol, 53% based on [PPh4]2[1]). Similarly, under the same reaction conditions, using CuBr, we have isolated a yellowish brown solid of [PPh4]2[3b] (80% based on [PPh4]2[1]) upon crystallization from Et2O/MeCN.

7787-70-4, 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.,7787-70-4 ,Copper(I) bromide, other downstream synthetic routes, hurry up and to see

Reference£º
Article; Shieh, Minghuey; Miu, Chia-Yeh; Liu, Yu-Hsin; Chu, Yen-Yi; Hsing, Kai-Jieah; Chiu, Jung-I; Lee, Chung-Feng; Journal of Organometallic Chemistry; vol. 815-816; (2016); p. 74 – 83;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, 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. Copper(I) bromide, cas is 7787-70-4,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

Synthesis of [(SIMes)CuBr]. In an oven-dried vial, copper(I) bromide (0.522 g, 3.63 mmol), SIMes.HCl (0.86 g, 2.52 mmol) and sodium tert-butoxide (0.243 g, 2.52 mmol) were loaded inside a glovebox and stirred in dry THF (18 mL) overnight at room temperature outside of the glovebox. After filtration of the reaction mixture through a plug of Celite, the filtrate was mixed with hexane to form a precipitate. A second filtration afforded 0.808 g (71% yield) of the title complex as an off-white solid.Spectroscopic and analytical data for [(SIMes)CuBr]: 1H NMR (300 MHz, [D6]acetone): delta=7.01 (s, 4H, HAr), 4.16 (s, 4H, NCH2), 2.37 (s, 12H, ArCH3), 2.29 (s, 6H, ArCH3); 13C NMR (75 MHz, CDCl3): delta=202.6 (C, NCN), 138.5 (C, CAr), 135.3 (CH, CAr), 135.0 (C, CAr), 129.7 (CH, CAr), 51.0 (CH2, NCH2), 21.0 (CH3, ArCH3), 18.0 (CH3, ArCH3); Elemental analysis calcd for C21H26BrCuN2 (449.89): C, 56.06; H, 5.83; N, 6.23. Found: C, 55.98; H, 5.64; N, 6.21%.

The chemical industry reduces the impact on the environment during synthesis,7787-70-4,Copper(I) bromide,I believe this compound will play a more active role in future production and life.

Reference£º
Patent; Institut Catala d’Investigacio Quimica; Institucio Catalana de Recerca i Estudis Avancats; US2009/69569; (2009); A1;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

Copper(I) bromide, cas is 7787-70-4, it is a common heterocyclic compound, the copper-catalyst compound, its synthesis route is as follows.,7787-70-4

General procedure: To a solution of (S,S)-iPr-pheboxH (0.051g, 0.173mmol) in dichloromethane (15mL), the corresponding copper(I) salt CuX (X=Cl, Br, I) (0.347mmol) was added and the mixture stirred at room temperature during 24h. Then, the reaction mixture was filtered via cannula, concentrated under reduced pressure to ca. 2mL and diethyl ether/n-hexane (1:2) (30mL) was added. The resulting solid was washed with n-hexane (3¡Á5mL) and vacuum-dried.

7787-70-4 is used more and more widely, we look forward to future research findings about Copper(I) bromide

Reference£º
Article; Vega, Esmeralda; De Julian, Eire; Borrajo, Gustavo; Diez, Josefina; Lastra, Elena; Gamasa, M. Pilar; Polyhedron; vol. 94; (2015); p. 59 – 66;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, 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. Copper(I) bromide, cas is 7787-70-4,the copper-catalyst compound, it is a common compound, a new synthetic route is introduced below.

General procedure: The complexes were typically obtained from the reaction of the copper halide (CuX) with the appropriate camphor ligand in THF (3 mL) upon stirring for ca. 18 h at room temperature. Filtration of the precipitate, washing with n-pentane (ca. 6mL) and drying under vacuum affords the Cu(I) complex.

Chemical properties determine the actual use. Each compound has specific chemical properties and uses. We look forward to more synthetic routes in the future to expand reaction routes of Copper(I) bromide, 7787-70-4

Reference£º
Article; Fernandes, Tiago A.; Mendes, Filipa; Roseiro, Alexandra P.S.; Santos, Isabel; Carvalho, M. Fernanda N.N.; Polyhedron; vol. 87; (2015); p. 215 – 219;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”