The Generation of the Ethenethiolate Anion and Its Reaction with Several Chloromethyl Alkyl Ethers and Sulfides
作者:Shigeo Tanimoto、Hideyuki Ikehira、Tatsuo Oida、Toshio Kokubo
DOI:10.1246/bcsj.56.1261
日期:1983.4
3-oxathiolane was deprotonated at the 4-position, followed by the cycloelimination of the resultant anion, leading to ethyl formate and the ethenethiolate anion. The anion was trapped by several chloromethyl alkyl ethers and sulfides to afford alkoxy(vinylthio)methanes and alkylthio(vinylthio)methanes respectively.
2-Ethoxy-1,3-oxathiolane 在 4-位被去质子化,随后生成的阴离子环消,生成甲酸乙酯和乙烯硫醇阴离子。阴离子被几种氯甲基烷基醚和硫化物捕获,分别得到烷氧基(乙烯基硫代)甲烷和烷硫基(乙烯基硫代)甲烷。