作者:Shigeo Jo、Shigeo Tanimoto、Toyonari Sugimoto、Masaya Okano
DOI:10.1246/bcsj.54.2120
日期:1981.7
The reaction of various phenols with 2-ethoxy-1,3-dithiolane proceeded smoothly in the presence of BF3·Et2O to afford 1,3-dithiolan-2-ylated phenols, which were readily hydrolyzed to the corresponding aldehydes. This process was also extended to N,N-dimethylaniline and indole.
各种苯酚与2-乙氧基-1,3-二硫杂环戊烷在BF3·Et2O的存在下顺利反应,生成1,3-二硫杂环戊烷-2-基化的苯酚,这些产物易于水解为相应的醛。这一过程也扩展到了N,N-二甲基苯胺和吲哚。