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CAS RN: 12354-84-6 | 產品號碼: P1763

(Pentamethylcyclopentadienyl)iridium(III) Dichloride Dimer


純度/分析方法: >95.0%(T)
别名:
  • Dichloro(pentamethylcyclopentadienyl)iridium(III) Dimer
文件:
1G
NT$11,088
≥100  14   下單後約2週內可以出貨

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* TCI會時常優化儲存條件,儲存溫度請以在線目錄為準,敬請留意。


產品號碼 P1763
純度/分析方法 >95.0%(T)
分子式 / 分子量 C__2__0H__3__0Cl__4Ir__2 = 796.69 
外觀與形狀(20°C) Solid
儲存條件 Room Temperature (Recommended in a cool and dark place, <15°C)
儲存在惰性氣體下 Store under inert gas
應避免的情況 Air Sensitive
包裝和容器 1G-Glass Bottle with Plastic Insert (閲覽圖片)
CAS RN 12354-84-6
PubChem Substance ID 87560398
MDL編號

MFCD00075435

產品規格
Appearance Light yellow to Brown powder to crystal
Purity(Argentometric Titration) min. 95.0 %
NMR confirm to structure
性質
GHS
相關法規
運輸資料
HS編碼* 2843.90-000
*此H.S.編碼用於日本出口報關, 不適用於您所在國家或地區的進口申報
Application
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


Application
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


考研文獻


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