Category: 7787-70-4

As a common heterocyclic compound, it belong copper-catalyst compound,Copper(I) bromide,7787-70-4,Molecular formula: BrCu,mainly used in chemical industry, its synthesis route is as follows.,7787-70-4

General procedure: [CuBr(CNR)3] (1-4). Any one of the isocyanides CNR (R=Xyl, 2-Cl-6-MeC6H3, 2-Naphtyl, Cy) (3.1mmol) was added to a suspension of CuBr (143mg, 1.0mmol) in chloroform (5mL) and the reaction mixture was stirred at RT for 1h. The solvent was removed in vacuo and the product was recrystallized by slow concentration of a CH2Cl2/hexane solution at RT to give colorless (1, 2, and 4) or orange (3) crystalline solid.

With the synthetic route has been constantly updated, we look forward to future research findings about Copper(I) bromide,belong copper-catalyst compound

Reference£º
Article; Melekhova, Anna A.; Novikov, Alexander S.; Luzyanin, Konstantin V.; Bokach, Nadezhda A.; Starova, Galina L.; Gurzhiy, Vladislav V.; Kukushkin, Vadim Yu.; Inorganica Chimica Acta; vol. 434; (2015); p. 31 – 36;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

As a common heterocyclic compound, it belong copper-catalyst compound,Copper(I) bromide,7787-70-4,Molecular formula: BrCu,mainly used in chemical industry, its synthesis route is as follows.,7787-70-4

General procedure: A solution of cuprous chloride (5.8 mg, 0.058 mmol) in acetonitrile(10 mL) was added dropwise to a well stirred solution of 1(30 mg, 0.058 mmol) in dichloromethane (10 mL) at room temperaturewith constant stirring. After stirring for 6 h, the solvent wasremoved under reduced pressure and the residue obtained wasfurther washed with petroleum ether to give 4 as white solid product.Yield

With the synthetic route has been constantly updated, we look forward to future research findings about Copper(I) bromide,belong copper-catalyst compound

Reference£º
Article; Bhat, Sajad A.; Mague, Joel T.; Balakrishna, Maravanji S.; Inorganica Chimica Acta; vol. 443; (2016); p. 243 – 250;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

7787-70-4, Copper(I) bromide is a copper-catalyst compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

7787-70-4, 2-(Carboxy-5-nitrophenyl)malonic acid dimethyl ester (8) A solution of 2-chloro-4-nitrobenzoic acid (75 g, 372 mmol) in dimethyl malonate (900 mL) was perfused with nitrogen for 15 min. Sodium methoxide (48.3 g, 894 mmol) was added in one portion and the contents exothermed to 48 C. Fifteen minutes later, copper (I) bromide (5.4 g, 37 mmol) was added in one portion and the contents were heated to 70 C. for 24 hrs. The reaction, which was 70% complete as determined by NMR, was subsequently heated to 85 C. for 5 hrs to completely consume the remaining 2-chloro4-nitrobenzoic acid. Water (900 mL) was added to the cooled reaction followed by hexanes (900 mL). The aqueous layer was separated, toluene (900 mL) was added, the mixture was filtered and aqueous layer separated. Fresh toluene (1800 mL) was added to the aqueous layer and the biphasic mixture acidified with 6N aqueous HCl (90 mL). A white precipitate formed and the contents were stirred for 18 hrs. The product was filtered off and dried to give a white solid (78.1 g, 70%) mp 153 C. 1 H NMR (DMSO) delta8.37 (d, J=2 Hz, 1H), 8.30 (d, J=1 Hz, 2H), 5.82 (s, 1H), 3.83 (s, 6H). 13 C NMR (DMSO) delta168.0, 167.3, 149.4, 137.1, 135.8, 132.5, 125.4, 123.7, 54.5, 53.4. Anal. Calcd for C11 H10 NO8: C, 48.49; H, 3.73; N, 4.71. Found: C, 48.27; H, 3.72; N, 4.76.

The synthetic route of 7787-70-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Pfizer Inc; US6121283; (2000); A;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.7787-70-4,Copper(I) bromide,as a common compound, the synthetic route is as follows.

7787-70-4, In a round bottom flask, copper(I) bromide (0.3mmol, 0.043g) was dissolved in 5mL of degassed MeCN. Under continuous stirring and in a N2-atmosphere, a 2mL degassed NCMe solution of HC(3,5-Me2pz)3 (0.33mmol, 0.1g) was added dropwise. The mixture was stirred at room temperature for 3h, then its volume was reduced to ca. 2mL by evaporation. Hexane (10mL) was added, and the obtained precipitate was filtered off and recrystallized from a mixture if CH2Cl2 and hexane (1:1) to afford complexes 3 as off-white powder. [CuBr(Tpm*)] (3): Yield (108.9mg) 82%. Elemental analysis calcd (%) for C16H22BrCuN6: C 43.49, H 5.02, N 19.02; found: C 43.45, H 5.51, N 19.62. FTIR (KBr): nu (cm-1)=3397m, 2962m, 2925m, 1562s, 1455s, 1412s, 1383s, 1303s, 1239s, 1153 w, 1112 w, 1035m, 980m, 905m, 845s, 824m, 796m, 695s. Far IR (CsI): nu (cm-1)=216m nu(Cu-Br). 1H NMR (300MHz, DMSO-d6, delta): 7.83 (s, 1H, HC(3,5-Me2pz)3), 6.04 (s, 3H, 4-H-pz), 2.40, 2.22 (s, s, 9H, 9H, 3,5-Me). 13C{1H} NMR (300MHz, DMSO-d6, delta): 149.12 (3-Cquat-pz), 140.28 (5-Cquat-pz), 106.44 (4-C-pz), 70.67 (HC(3,5-Me2pz)3), 13.48,10.37 (3,5-Me). ESI(+)MS in MeCN (m/z assignment, % intensity): 204 ({[HC(3,5-Me2pz)3]Cu+MeCN}+, 100), 361 ({[HC(3,5-Me2pz)3]Cu}+, 26).

As the paragraph descriping shows that 7787-70-4 is playing an increasingly important role.

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”

As a common heterocyclic compound, it belong copper-catalyst compound,Copper(I) bromide,7787-70-4,Molecular formula: BrCu,mainly used in chemical industry, its synthesis route is as follows.,7787-70-4

General procedure: HLBAP (0.525 g, 1 mmol) and triethylamine (0.28 mL, 2 mmol) were dissolved in a 2:1 acetonitrile/dichloromethane mixture (45 ml), and then copper salt with the corresponding anion (1 mmol) was added. The reaction mixture was stirred for 4 h at room temperature in the presence of air. X-ray quality red brown crystals were grown from a 1:1 solvent mixtureof dichloromethane/methanol.

With the synthetic route has been constantly updated, we look forward to future research findings about Copper(I) bromide,belong copper-catalyst compound

Reference£º
Article; Safaei, Elham; Bahrami, Hadiseh; Wojtczak, Andrzej; Alavi, Saman; Jagli?i?, Zvonko; Polyhedron; vol. 122; (2017); p. 219 – 227;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.7787-70-4,Copper(I) bromide,as a common compound, the synthetic route is as follows.,7787-70-4

General procedure: Compound 5c was prepared as described for 5a. In this respect, 2 (100 mg, 0.160 mmol) was reacted with [CuBr] (3c) (23 mg, 0.160 mmol). Appropriate work-up, gave 5c (111 mg, 0.144 mmol, 90% based on 2) as a brown solid Mp.: 180 C. IR (KBr, cm-1): nuC?C 1983 (w). 1H NMR (d6-DMSO, delta): 0.24 (s, 9 H, SiMe3), 0.30 (s, 9 H, SiMe3), 7.61 (ddd, 3JH7H6 = 4.7 Hz, 3JH7H8 = 7.3 Hz; 1 H, H7), 7.95 (ddd, 3JH2H1 = 6.3 Hz, 3JH2H3 = 6.6 Hz; 1 H, H2), 8.07 (ddd, 4JH8H6 = 1.5 Hz, 3JH8H7 = 7.3 Hz, 3JH8H9 = 7.8 Hz; 1 H, H8), 8.43 (m, 4JH3H1 = 1.0 Hz, 3JH3H2 = 6.6 Hz; 3JH3H4 = 8.0 Hz, 3JH9H8 = 7.8 Hz; 2 H, H3, H9), 8.67 (dd, 3JH6H7 = 4.7 Hz, 4JH6H8 = 1.5 Hz, 1 H, H6), 8.85 (d, 3JH4H3 = 8.0 Hz, 1 H, H4), 9.05 (dd, 3JH1H2 = 6.3 Hz, 1 H, 4JH1H3 = 1.0 Hz, 1 H, H1), 9.95 (s, 1 H, H5), 10.06 (s, 1 H, H10). ESI-MS (m/z (rel. intens.) in thf: [M++Br] 687 (100), [M+-CuBr + K] 662 (25). Anal. Calc. for C24H28N4CuBrPtSi2 (767.21 g/mol): C, 37.57; H, 3.67; N, 7.30. Found: C, 37.68; H, 3.63; N, 6.92%.

As the paragraph descriping shows that 7787-70-4 is playing an increasingly important role.

Reference£º
Article; Al-Anber, Mohammed; Wetzold, Nora; Walfort, Bernhard; Rueffer, Tobias; Lang, Heinrich; Inorganica Chimica Acta; vol. 398; (2013); p. 124 – 131;,
Copper catalysis in organic synthesis – NCBI
Special Issue “Fundamentals and Applications of Copper-Based Catalysts”