作者:C. Ainsworth、Yu-Neng Kuo
DOI:10.1016/s0022-328x(00)90476-5
日期:1972.12
methods are described for the preparation of alkyl, dialkyl, aryl and diaryl ketene bis(trialkylsilyl)acetals. One is by reaction of αmetalated trimethylsilyl carboxylates with trimethylchlorosilane (TMCS) and the otehr is by inteaction of dianions of carboxylic acids and TMCS. The dianion of cyclopropane carboxylic acid and TMCS gave C-silated ester in 90% yield. Pyrolysis of diphenyl ketene bis(trialkylsilyl)
描述了两种高产率的合成方法,用于制备烷基,二烷基,芳基和二芳基乙烯酮双(三烷基甲硅烷基)缩醛。一种是通过α金属化的三甲基甲硅烷基羧酸盐与三甲基氯硅烷(TMCS)的反应,而另一种是通过羧酸与TMCS的二价阴离子的相互键合。环丙烷羧酸和TMCS的二价阴离子以90%的收率得到C-硅酸酯。交叉实验表明,二苯基乙烯酮双(三烷基甲硅烷基)缩醛热解为二苯基乙烯酮和双(三烷基甲硅烷基)醚在分子间进行。单取代的和二烷基酮烯(三甲基甲硅烷基)缩醛的热解得到了酮烯-酮缩醛的加成产物(III),其在溶剂分解时以高收率提供了β-酮酸。给出了许多化合物的NMR和质谱数据。