<p>Thienoacenes are significant compounds as organic materials. One of the most efficient ways to synthesize thienoacenes is to form multiple C–S bonds in a single step. Because unprotected S–H bonds are easily oxidized to S–S bonds, <i>S</i>-Me protected substrates are commonly used for the purpose. However, their reactivity is insufficient, and one-step construction of multiple C–S bonds is still challenging. We herein report the electrochemical synthesis of thienoacenes from <i>S</i>-methoxymethyl (MOM)-protected diarylacetylenes. In the presence of Bu<sub>4</sub>NBr as a halogen mediator, electrochemical double C–S cyclization of diarylacetylenes bearing two MOM groups proceeded to afford [1]benzothieno[3,2-<i>b</i>][1]benzothiophene (BTBT) derivatives. While <i>S</i>-Me or <i>S</i>-<i>p</i>-methoxybenzyl (PMB)-protected diarylacetylenes did not afford BTBT, BTBT was selectively obtained when a substrate protected with <i>S</i>-MOM groups was used. The <i>S</i>-MOM protection strategy is also effective for the electrochemical synthesis of a more π-expanded thienoacene such as dibenzo[<i>d</i>,<i>d</i><sup>′</sup>]thieno[3,2-<i>b</i>,4,5-<i>b</i>′]dithiophene (DBTDT).</p><p></p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Synthesis of thienoacenes by electrochemical double C–S cyclization using a halogen mediator

  • Koichi Mitsudo,
  • Takuya Nagahara,
  • Nozomi Kataura,
  • Yuka Okamura,
  • Toki Yonezawa,
  • Yuri Tachibana,
  • Nolan Soulié,
  • Keisuke Shigemori,
  • Eisuke Sato,
  • Hiroki Mandai,
  • Seiji Suga

摘要

Thienoacenes are significant compounds as organic materials. One of the most efficient ways to synthesize thienoacenes is to form multiple C–S bonds in a single step. Because unprotected S–H bonds are easily oxidized to S–S bonds, S-Me protected substrates are commonly used for the purpose. However, their reactivity is insufficient, and one-step construction of multiple C–S bonds is still challenging. We herein report the electrochemical synthesis of thienoacenes from S-methoxymethyl (MOM)-protected diarylacetylenes. In the presence of Bu4NBr as a halogen mediator, electrochemical double C–S cyclization of diarylacetylenes bearing two MOM groups proceeded to afford [1]benzothieno[3,2-b][1]benzothiophene (BTBT) derivatives. While S-Me or S-p-methoxybenzyl (PMB)-protected diarylacetylenes did not afford BTBT, BTBT was selectively obtained when a substrate protected with S-MOM groups was used. The S-MOM protection strategy is also effective for the electrochemical synthesis of a more π-expanded thienoacene such as dibenzo[d,d]thieno[3,2-b,4,5-b′]dithiophene (DBTDT).