Potential Radiation Protective Agents V. Synthetic Approaches to 2-Aryl-2-Mercaptoethylamines
作者:Beng-Thong Ho、Walter C. McCarthy
DOI:10.1002/jps.2600560524
日期:1967.5
Abstract β-Acetthiohydrocinnamoyl azide, through the Curtius degradation, gave 2-mercapto-2-phenylethylamine hydrochloride in low yield. Following the nitro-thiolacetate route to 2-aryl-2-mercaptoethylamines, two acetoxy-substituted β -nitrostyrenes were found to undergo an anomalous reaction with thiolacetic acid involving reduction of the nitro group, formation of elemental sulfur, and the isolation
摘要β-乙硫基氢肉桂酰基叠氮化物经Curtius降解,低收率得到2-巯基-2-苯基乙胺盐酸盐。继硝基硫醇乙酸盐途径生成2-芳基-2-巯基乙胺后,发现两个乙酰氧基取代的β-硝基苯乙烯与硫代乙酸发生异常反应,包括硝基还原,元素硫的形成以及含比起始原料多四个乙酰基。