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CAS RN: 12354-84-6 | 產(chǎn)品編碼: P1763

(Pentamethylcyclopentadienyl)iridium(III) Dichloride Dimer


純度/分析方法: >95.0%(T)
別名:
  • (五甲基環(huán)戊二烯基)二氯化銥(III)二聚體
  • 二氯(五甲基環(huán)戊二烯基)合銥(III)二聚體
  • Dichloro(pentamethylcyclopentadienyl)iridium(III) Dimer
產(chǎn)品文檔:
100MG
¥390.00
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250MG
¥750.00
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1G
¥1,890.00
2   1   ≥40 
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產(chǎn)品編碼 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) 固體
儲存溫度 室溫 (15°C以下陰涼干燥處)
儲存在惰性氣體下 存放于惰性氣體之中
應(yīng)避免的情況 空氣
包裝和容器 1G-帶有塑料內(nèi)管的玻璃瓶 (查看圖片)
CAS RN 12354-84-6
PubChem物質(zhì)ID 87560398
MDL編號

MFCD00075435

技術(shù)規(guī)格
Appearance Light yellow to Brown powder to crystal
Purity(Argentometric Titration) min. 95.0 %
NMR confirm to structure
物性(參考值)
GHS
相關(guān)法規(guī)
新化學(xué)物質(zhì)備案回執(zhí)號 B1A232215218
運(yùn)輸信息
監(jiān)管條件代碼(*)
應(yīng)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


應(yīng)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


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