Addition of Trichlorosilane to Styrene, 2 Vinylpyridine, Allylcyanide and Octene-1
作者:Shun’ichi Nozakura
DOI:10.1246/bcsj.29.784
日期:1956.7
Addition reactions of trichlorosilane to styrene, 2-vinylpyridine, allylcyanide, and octene-1 were attempted in the presence of bases such as pyridine and in the presence of tetrapyridine nickel(II) chloride. The structures of the reaction products were established. In the presence of bases, trichlorosilane was added to 2-vinylpyridine and allylcyanide, yielding 2-β-trichlorosilylethylpyridine and
在吡啶等碱和四吡啶氯化镍 (II) 存在下,尝试了三氯硅烷与苯乙烯、2-乙烯基吡啶、烯丙基氰化物和辛烯-1 的加成反应。建立了反应产物的结构。在碱存在下,将三氯硅烷加入到 2-乙烯基吡啶和烯丙基氰化物中,分别生成 2-β-三氯甲硅烷基乙基吡啶和 β-三氯甲硅烷基丁腈。另一方面,在四吡啶氯化镍存在下,对所有检测的乙烯基化合物进行添加。(没有尝试2-乙烯基吡啶。)然而,在这种情况下,证明加成产物由两种位置异构体组成,其发生是由于加成方向不同,对于每种起始乙烯基化合物。