Butadiene sulphone chemistry. Part III. Condensation reactions of butadiene sulphone
作者:C. S. Argyle、K. G. Mason、M. A. Smith、E. S. Stern
DOI:10.1039/j39670002176
日期:——
2,5-Dihydrothiophen dioxide reacts with aliphatic ketones to give di-condensation products [e.g., (II)] and monosubstitution products [e.g., (III) and (IV)] with a carbinol group either at the 5- or at the 4-position. The structures are confirmed by physical means and independent syntheses of the hydrogenated carbinols. From aromatic aldehydes the di-condensation products only are obtained. Acrylonitrile
2,5-二氢噻吩二氧化物与脂肪族酮反应,生成在5或4处带有甲醇基团的二缩合产物[例如(II)]和单取代产物[例如(III)和(IV)]。 -位置。通过物理手段和氢化甲醇的独立合成证实了结构。从芳族醛仅获得缩合产物。丙烯腈与2,5-二氢噻吩二氧化物反应生成四氰基乙基化产物(V),该产物容易消除二氧化硫而生成二烯(VI)。通过与肼水溶液加热从(II)中除去二氧化硫的新方法得到了带有二硫化氢的二肼基二烯(VII)。