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CAS RN: 1058661-78-1 | 产品编码: C2347
Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)]
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![Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)]](/_ui/responsive/theme-tci/images/missing_product_zoom.jpg "Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)]")
| 产品编码 | C2347 |
| 纯度/分析方法 | >98.0%(T) |
| 分子式/分子量 | C__3__0H__3__6ClN__3Pd = 580.51 |
| 外观与形状（20°C） | 固体 |
| 储存温度 | 室温 (15°C以下阴凉干燥处) |
| 包装和容器 | 1G-Glass Bottle with Plastic Insert （查看图片）, 200MG-Glass Bottle with Plastic Insert （查看图片） |
| CAS RN | 1058661-78-1 |
| PubChem物质ID | 87560979 |
技术规格
| Appearance | White to Almost white powder to crystal |
| Purity(Argentometric Titration) | min. 98.0 % |
| Purity(Chelometric back titration) | min. 98.0 % |
物性（参考值）
GHS
相关法规
运输信息
| HS编码* | 2843.90-000 |
应用
N-Heterocyclic Carbene (NHC) Palladium Complex Catalyst
References
- Practical Heck?Mizoroki coupling protocol for challenging substrates mediated by an N-heterocyclic carbene-ligated palladacycle
- N-Heterocycle carbene (NHC)-ligated cyclopalladated N,N-dimethylbenzylamine: a highly active, practical and versatile catalyst for the Heck?Mizoroki reaction
应用
SingaCycle(TM)-E1 –Catalyst for the Heck-Mizoroki Reaction
Typical procedure: Aryl Bromide (1 mmol), olefin (1.2 mmol), K2CO3 (2.0 mmol) and 2 mol% NMP solution of SingaCycle(TM)-E1 (400 µL) are added to a vial with a magnetic stir bar. The atmosphere above the reaction mixture is purged with Ar over 30 sec. The vial is closed with a screw cap, and heated at 140°C with vigorous stirring over 18 h. After cooling, the reaction mixtures are filtered under dilution with CH2Cl2 (total: 20 mL). The crude product is loaded directly over a short pad of silica gel and purified by flash chromatography.
References
- E. A. B. Kantchev, G.-R. Peh, C. Zhang, J. Y. Ying, Org. Lett. 2008, 10, 3949.
- G.-R. Peh, E. A. B. Kantchev, C. Zhang, J. Y. Ying, Org. Biomol. Chem. 2009, 7, 2110.
- J. Y. Ying, E. A. B. Kantchev, PCT Int Appl. WO 2008156451 2008.
- E. A. B. Kantchev, J. Y. Ying, Organometallics 2009, 28, 289.
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