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CAS RN: 12354-84-6 | 产品编码: P1763

(Pentamethylcyclopentadienyl)iridium(III) Dichloride Dimer


纯度/分析方法: >95.0%(T)
别名:
  • (五甲基环戊二烯基)二氯化铱(III)二聚体
  • 二氯(五甲基环戊二烯基)合铱(III)二聚体
  • Dichloro(pentamethylcyclopentadienyl)iridium(III) Dimer
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100MG
¥410.00
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250MG
¥850.00
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1G
¥3,320.00
5   1   ≥100 
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产品编码 P1763
纯度/分析方法 >95.0%(T)
分子式/分子量 C__2__0H__3__0Cl__4Ir__2 = 796.69 
外观与形状(20°C) 固体
储存温度 室温 (15°C以下阴凉干燥处)
储存在惰性气体下 存放于惰性气体之中
应避免的情况 空气
包装和容器 100MG-带有塑料内管的玻璃瓶 (查看图片),  1G-带有塑料内管的玻璃瓶 (查看图片)
CAS RN 12354-84-6
PubChem物质ID 87560398
MDL编号

MFCD00075435

技术规格
Appearance Light yellow to Brown powder to crystal
Purity(Argentometric Titration) min. 95.0 %
NMR confirm to structure
物性(参考值)
GHS
相关法规
新化学物质备案回执号 B1A232215218
运输信息
监管条件代码(*)
应用
Synthesis of N―H Carbazoles via Ir-catalyzed Intramolecular C―H Amination

P1763,C2346,P0461

Typical Procedure:
To a 20 mL two-necked flask with a reflux condenser and a rubber cap are added 2-aminobiphenyls (0.5 mmol), [Cp*IrCl2]2 (0.01 mmol, 8.0 mg), Cu(OAc)2 (0.1 mmol, 18 mg), pivalic acid (1 mmol, 102 mg), 1-methylnaphthalene (ca. 30 mg) as an internal standard, and N-methyl-2-pyrrolidone (NMP, 3 mL). Then, the resulting mixture is stirred under air at 120 °C for 3-6 h. After cooling, the reaction mixture is extracted with ethyl acetate (100 mL). The organic layer is washed by aqueous NaHCO3 (100 mL×3), and dried over Na2SO4. After evaporation of the solvents under vacuum, the product is isolated by column chromatography on silica gel using hexane-ethyl acetate (10:1) as the eluent.

References


应用
Iridium-Catalyzed Redox-Neutral Alcohol-Amine Coupling on Kilogram Scale

Typical procedure: An 8L Hastelloy pressure reactor is charged with the alcohol (2.4 kg), 3-chloro-4-fluorobenzylamine (2.97 kg), (pentamethylcyclopentadienyl)iridium(III) dichloride dimer (3.7 g), 1 N aqueous sodium bicarbonate solution (9.2 mL) and toluene (470 mL). The reactor is purged with nitrogen and then sealed and heated to 110 °C and held for 24 h. The maximum internal pressure during the reaction is 25 psig. After 24 h, an additional charge of the iridium catalyst (1.42 g) and the sodium bicarbonate solution (3.5 mL) is added to the mixture, which is heated to 110 °C for 16 h. The mixture is cooled and diluted with 2-propanol (7.2 L), and distilled under reduced pressure. When the pot volume reached ~7 L, 2-propanol (7.2 L) is added, and distillation is continued, again reducing the volume to ~7 L. After a second dilution with 2-propanol (7.2 L), the mixture is concentrated to 7L, cooled to ambient temperature, and transferred into a reactor containing a preheated (50 °C) solution of 5 N HCl in 2-propanol (9.31 kg, 2.75 eq.). The resulting slurry is cooled to ambient temperature and granulates for 4 h. The resulting product is removed by filtration, washed with 2-propanol (72 L), and dried in a vacuum oven (50 °C, 0.05 bars) to give the desired product (4.81 kg, 76%) as a white crystalline powder (m.p. 232 °C) including 4 ppm of Ir.

References


PubMed Literature


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