1,3-二(2,6-二异丙基苯基)氯化咪唑

• 产品号: H27150
• CAS号: 250285-32-6
• 分子式: C27H37ClN2
• 分子量: 425.04908
• 纯 度: 97%

产品别名

• 标题: 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride
• IUPAC标准名: 1,3-bis[2,6-bis(propan-2-yl)phenyl]-3H-1λ^5-imidazol-1-ylium chloride
• IUPAC传统名: 1,3-bis(2,6-diisopropylphenyl)-1λ^5-imidazol-1-ylium chloride

产品登记号

• MDL号: MFCD02684545
• CAS号: 250285-32-6

产品性质

• 纯度: 97%
• 熔点: ca 280°C dec.
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• GHS警示性声明: P261-P305+P351+P338-P302+P352-P321-P405-P501A
• 危险公开号: 36/37/38
• 安全公开号: 26-37
• 保存注意事项: Hygroscopic
• TSCA收录: 否

参考文献

• In the presence of a base such as KO-t-Bu, generates the imidazol-2-ylidene, an example of an N-heterocyclic carbene (NHC). NHCs are relatively strong bases, and valuable replacements for phosphine ligands in transition metal chemistry. They are relatively stable to dimerization, but sensitive to air and moisture, so are best generated in situ. Review: Angew. Chem. Int. Ed., 36, 2163 (1997). For a review of stable carbenes, see: Chem. Rev., 100, 39 (2000).
• Used as a phosphine-free ligand in various metal-catalyzed coupling reactions, often with advantageous results in difficult cases. For use in the Pd-catalyzed cross-coupling of aryl Grignards with aryl chlorides (Kumada reaction), see: J. Am. Chem. Soc., 121, 9889 (1999). For Pd-catalyzed coupling of trimethoxysilanes with electron-deficient aryl chlorides, see: Org. Lett., 2, 2053 (2000). Many examples have been recorded of the use of NHC ligands in the Suzuki coupling reaction, for examples utilizing 1,3-bis(2,6-diisopropylphenyl)imiazol-2-ylidene, enabling otherwise difficult coupling reactions of aryl chlorides with aryl and alkyl boronic acids, see: Synlett, 292 (2001) (includes alkylboronic acids: better yields than 1,3-dimesitylimidazol-2-ylidene); Org. Lett., 6, 4435 (2004); Tetrahedron Lett., 45, 3511 (2004).
• See also 1,3-Dimesitylimidazolium chloride, H27535.