作者:Natalia A. Keiko、Ludmila G. Stepanova、Ekaterina A. Verochkina、Yurii A. Chuvashev
DOI:10.3998/ark.5550190.0012.a11
日期:——
allowing alkylthioethanals to be synthesized in 80-93% yields, has been developed. It comprises the hydrolysis of bis-1,1-alkoxy-2-alkylthioethanes using two-phase system water organic solvent. The method is applicable for both common aldehydes bearing lower radicals (R = Pr, Bu) and hitherto unknown highly boiling aldehydes (R = C7H15, C8H17, PhCH2). It has been found that alkylthioethanals can spontaneously
已经开发出一种方法,可以以 80-93% 的产率合成烷基硫乙醛。它包括使用两相系统水有机溶剂水解双-1,1-烷氧基-2-烷基硫代乙烷。该方法适用于带有低级自由基的常见醛 (R = Pr, Bu) 和迄今为止未知的高沸点醛 (R = C7H15, C8H17, PhCH2)。已经发现烷基硫代乙醛可以自发地三聚成 2,4,6-烷基硫代三恶烷。在碱性介质(1N NaOH、KF/Si(OEt)4/EtOH)中,烷硫醇以高达 60% 的产率( 1 H NMR)提供羟醛自缩合产物。在丁硫基-和烷氧基乙醛与呋喃-或噻吩-2-甲醛的竞争性相互作用(交叉羟醛缩合)中,含硫碳负离子的反应性比烷氧基类似物高六倍以上。