New learning discoveries about 54761-04-5

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various fields.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

54761-04-5, General procedure: A mixture of Ce(OTf)3 (0.1388g, 0.2mmol) and C12H8N2 (phen) (0.005g) was dissolved in a mixture of CH3CN (10ml) and DMF (three drops). After the mixture was stirred for 1h, the ligand L (0.2752g, 0.8mmol) was added to this mixture. Stirring was continued for 4h at ambient temperature. After this time, any insoluble residues were removed by filtration, and the filtrate was evaporated slowly at room temperature for about one month to yield colorless crystalline products.

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various fields.

Reference£º
Article; Xu, Shan; Liu, Min; Yang, Yu-Ping; Jiang, Yu-Han; Li, Zhong-Feng; Jin, Qiong-Hua; Wang, Xin; Xue, Xiao-Nan; Polyhedron; vol. 87; (2014); p. 293 – 301;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Analyzing the synthesis route of 54761-04-5

As the paragraph descriping shows that 54761-04-5 is playing an increasingly important role.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

54761-04-5, General procedure: These were all prepared in the same way: the example given for Ir?Eu is typical. A mixture of Ir?A (0.043g, 0.04mmol) and Eu(OTf)3 (0.024g, 0.04mmol) in anhydrous MeOH under Ar was stirred for 30min. To this was slowly added a solution of NaOH (1M in MeOH) such that the apparent pH was maintained at 5. The reaction mixture was then heated to 50C with constant stirring for 48h. After cooling the reaction mixture the solvent was evaporated under reduced pressure. The residue was dissolved in minimum amount of MeOH and re-precipitated by the gradual addition of ether. This dissolution/re-precipitation process was repeated several times and the light yellow solid mass was collected by filtration to give Ir?Eu in 60-70% yield.

As the paragraph descriping shows that 54761-04-5 is playing an increasingly important role.

Reference£º
Article; Jana, Atanu; Pope, Simon J.A.; Ward, Michael D.; Polyhedron; vol. 127; (2017); p. 390 – 395;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Simple exploration of 54761-04-5

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.54761-04-5,Ytterbium(III) trifluoromethanesulfonate,as a common compound, the synthetic route is as follows.

Under the protection of nitrogen atmosphere, the amount of organic solvent (for the volume ratio of 1: 0.2 of a mixture of polyethylene glycol and 15-crown-5) was added 100 mmol of the compound of formula (I) 250 mmol of the compound of formula (II) above, 9 mmol of catalyst (3 mmol Pd(dba)2) With 6mmol A mixture of ytterbium trifluoromethanesulfonate ,12 mmol oxidizer silver acetate and 30 mmol accelerator N-n-butyl-N-methylpiperidine bis(trifluoromethanesulfonyl)imide salt, and then the temperature was raised to 70 C, and the reaction was stirred at that temperature for 6 hours. After the reaction is complete, the filtrate is adjusted to adjust the pH of the filtrate to neutral and then saturated with hydrogen carbonate Sodium aqueous solution is fully shaken washing, adding dichloromethane extraction, separation of organic phase, and then Dried over anhydrous sodium sulfate, concentrated under reduced pressure, the residue over 200-300 mesh silica gel column chromatography, in vivo A mixture of petroleum ether and acetone having a ratio of 1: 3 was used as the eluent to give a compound of formula (III) And the yield was 93.9%., 54761-04-5

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Henan Academy Of Sciences Chemical Institute Co., Ltd.; Huo Cuimeng; Fu Yang; Chen Jin; Zhang Xin; Zhao Yongde; (9 pag.)CN105037081; (2016); B;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Some tips on 54761-04-5

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

54761-04-5, General procedure: ReBr(CO)3(N,N’-Phd-O,O’)Ln(OTf)3(THF) (III Y, Ln = Y; III Eu, Ln = Eu; III Yb, Ln = Yb) heterobimetallic complexes were synthesised by allowing 1.0 mmol (0.560 g) of fac-ReBr(CO)3(Phd) to react with 1.0 mmol of the respective anhydrous triflate salt Ln(OTf)3 in 20 mL of THF. After 72 h of stirring at ambient temperature, the solvent was evaporated under reduced pressure and diethyl ether (10 mL) was added. The solid thus separated was filtered, washed with a small amount of diethyl ether and dried.

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Bortoluzzi, Marco; Battistel, Dario; Albertin, Gabriele; Daniele, Salvatore; Enrichi, Francesco; Rumonato, Riccardo; Chemical Papers; vol. 70; 1; (2016); p. 43 – 52;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

New learning discoveries about 54761-04-5

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various fields.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,54761-04-5

General procedure: Compounds Ir6Ln (Ln=Eu, Tb, Er, Yb) were synthesized under similar optimized experimental conditions. A typical procedure for the preparation of [EuIr6(ppy)12(bpp)2(bppH)4](CF3SO3)¡¤18H2O (Ir6Eu) is described as below. Eu(CF3SO3)3 (0.0120g, 0.02mmol) was added to a methanol solution (5cm3) of [Ir(ppy)2(bppH)] (0.0135g, 0.02mmol). After heating the yellow solution at 100C under microwave irradiation for 30min, the filtrate was left to stand for one week at room temperature. Yellow block crystals were collected by suction filtration, washed with a minimum amount of methanol.

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various fields.

Reference£º
Article; Zeng, Dai; Fan, Kun; Wang, Lu-Ping; Bao, Song-Song; Ren, Min; Zheng, Li-Min; Journal of Magnetism and Magnetic Materials; vol. 484; (2019); p. 139 – 145;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Simple exploration of 54761-04-5

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.54761-04-5,Ytterbium(III) trifluoromethanesulfonate,as a common compound, the synthetic route is as follows.,54761-04-5

4.6. Synthesis of a Complex of H3TTPTCN and Ytterbium A solution of 30.5 mg (0.05 mmol) of ytterbium triflate in 1 ml of water is admixed with a solution of 36 mg (0.05 mmol) of H3TTPTCN in 2 ml of water in which the pH is adjusted to 7 by addition of an aqueous NaOH solution. The subsequent procedure is as described in section 4.2 above. In this way a complex is isolated: [Yb(TTPTCN)].6.5H2O (yield: 30%). Elemental analysis: calculated (found): C: 33.55% (33.69%) H: 4.38% (4.37%) N: 26.08% (25.61%)

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Giraud, Marion; Demadrille, Renaud; Mazzanti, Marinella; Andreiadis, Eugen Sorin; US2011/112289; (2011); A1;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Some tips on 54761-04-5

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated,54761-04-5

Example 6 2-(4-{3-[5-Acetyl-3-(4-trifluoromethyl-phenyl)-4,5,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-1-yl]-2-hydroxy-propyl}-piperazin-1-yl)-benzonitrile. A solution of 1-[1-oxiranylmethyl-3-(4-trifluoromethyl-phenyl)-1,4,6,7-tetrahydro-pyrazolo[4,3-c]pyridin-5-yl]-ethanone (0.84 g, 2.30 mmol) in CH2Cl2 (10 mL) was treated with ytterbium(III) triflate (0.29 g, 0.46 mmol) and 1-(2-cyanophenyl)-piperazine (0.75 g, 3.5 mmol) at 25 C. and stirred for 48 h before it was diluted with CH2Cl2 (100 mL) and H2O (50 mL). The organic layer was separated, washed with H2O (2*50 mL), dried over Na2SO4, and concentrated. Column chromatography (silica, 5% MeOH/CH2Cl2) afforded 1.15 g (90%) of light yellow crystals. TLC (silica, 10% MeOH/CH2Cl2): Rf=0.30. MS (electrospray): m/z 553.3 ([M+H]+, C29H31F3N6O2 requires 552.3). 1H NMR (CDCl3, 400 MHz, a mixture of two rotamers): 7.82 and 7.68 (AB pattern, Jab=8.2 Hz, 2H), 7.76 and 7.72 (AB pattern, Jab=8.4 Hz, 2H), 7.60-7.48 (m, 2H), 7.05-7.00 (m, 2H), 4.90 and 4.78 (AB pattern, Jab=16 Hz, 1H), 4.69 (s, 1H), 4.30-3.71 (m, 6H), 3.25 (m, 4H), 3.02-2.75 (m, 4H), 2.70-2.65 (m, 2H), 2.60-2.53 (m, 2H), 2.23 (s, 1.5H), 2.18 (s, 1.5H).

The synthetic route of 54761-04-5 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Breitenbucher, J. Guy; Cai, Hui; Edwards, James P.; Grice, Cheryl A.; Gu, Yin; Gustin, Darin J.; Karlsson, Lars; Khatuya, Haripada; Meduna, Steven P.; Pio, Barbara A.; Sun, Siquan; Tays, Kevin L.; Thurmond, Robin L.; Wei, Jianmei; US2003/69240; (2003); A1;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Downstream synthetic route of 54761-04-5

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.54761-04-5,Ytterbium(III) trifluoromethanesulfonate,as a common compound, the synthetic route is as follows.

To 5 (0.131 g, 1.0 mmol) and Yb(OTf)3 (0.124 g, 0.20 mmol) in CH2Cl2 (1.5 mL) under argon was added methyl vinyl ketone 22(0.162 mL, 2 mmol). The reaction mixture was stirred at rt overnight and concentrated in vacuo. Purification by silica gel chromatography (1:1, EtOAc:hexane, to 100%, EtOAc, as eluent) afforded 24 asa white solid (0.051 g, 25%) and 23 as a yellow oil (0.128 g, 37%): Rf.0.23 (1:1, EtOAc:methanol, as eluent); 1H NMR (700 MHz, CDCl3)d 9.12 (br s, 1H), 7.87 (dd, J7.6, 1.1 Hz, 1H), 7.72 (td, J7.6, 1.1 Hz,1H), 7.47 (td, J7.6, 1.1 Hz, 1H), 7.35 (dd, J7.6, 1.1 Hz, 1H), 4.32 (t,J6.0 Hz, 2H), 4.14 (t, J8.1 Hz, 2H), 3.29 (t, J6.0 Hz, 2H), 3.27 (t,J8.1 Hz, 2H), 2.23 (s, 3H) ppm; 13C NMR (176 MHz, CDCl3) d 206.2,168.1, 138.6, 136.4, 134.7, 128.7 (q, J285 Hz), 124.7, 121.9, 119.4,116.8, 55.6, 49.2, 40.1, 30.1, 25.5; IR nmax (thin film) 1714 (C]O),1661 (C]N) cm1; LRMS (TOF ES), 203.5 (100%) [MH], 201.7(70%), 132.1 (25%); LRMS (TOF ES-), 149.0 (100%) [OTf]; HRMS(FTMS ES) calculated for C13H15NOH, 202.12264; found202.12262; HRMS (FTMS ES-), calculated for CF3O3Se, 148.95257;found 148.95217.

54761-04-5 Ytterbium(III) trifluoromethanesulfonate 2733225, acatalyst-ligand compound, is more and more widely used in various.

Reference£º
Article; Girling, P. Ricardo; Batsanov, Andrei S.; Calow, Adam D.J.; Shen, Hong C.; Whiting, Andrew; Tetrahedron; vol. 72; 8; (2016); p. 1105 – 1113;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI

Analyzing the synthesis route of 54761-04-5

As the paragraph descriping shows that 54761-04-5 is playing an increasingly important role.

54761-04-5, Ytterbium(III) trifluoromethanesulfonate is a catalyst-ligand compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Example 2 Preparation of Ru(OTf)[(S,S)-Tsdpen](p-cymene) as Sulfonate Complex First, Ru[(S,S)-Tsdpen](p-cymene) (180 mg, 0.3 mmol), Yb(OTf)3 (183 mg, 0.3 mmol) (manufactured by Aldrich), and 3 ml of CH3OH were charged in a 20 ml Schlenk-type reaction tube purged with argon. Then, the resultant mixture was degassed and stirred at room temperature for 10 minutes. After CH3OH was distilled off under reduced pressure (1 mm Hg), 2 ml of THF was added to the residue, and the produced precipitate was filtered off, washed with 1 ml of THF and with 5 ml of toluene, and dried under reduced pressure (1 mmHg) to obtain 130 mg of Ru(OTf)[(S,S)-Tsdpen](p-cymene).

As the paragraph descriping shows that 54761-04-5 is playing an increasingly important role.

Reference£º
Patent; NAGOYA INDUSTRIAL SCIENCE RESEARCH INSTITUTE; US2008/234525; (2008); A1;,
Metal catalyst and ligand design
Ligand Template Strategies for Catalyst Encapsulation – NCBI