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2020 , Vol. 40 >Issue 5: 1257 - 1265

DOI: https://doi.org/10.6023/cjoc201911036

研究论文

硫酸催化的炔丙醇快速亲核取代反应

  • 张顺吉 ,
  • 刘会丽
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  • 淮北师范大学化学与材料科学学院 安徽淮北 235000

收稿日期: 2019-11-27

  修回日期: 2020-01-06

  网络出版日期: 2020-01-21

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Sulfuric Acid Catalyzed Rapid Nucleophilic Substitution of Propargyl Alcohols

  • Zhang Shunji ,
  • Liu Huili
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  • Department of Chemistry, Huaibei Normal University, Huaibei, Anhui 235000

Received date: 2019-11-27

  Revised date: 2020-01-06

  Online published: 2020-01-21

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摘要

硫酸有效地催化炔丙醇和一系列碳和氧亲核试剂的直接亲核取代反应以形成碳-碳键和碳-氧键.反应可以在未除水溶剂中和空气条件下进行并获得良好的产率.室温下大多数底物的反应能在1 min内完成.

关键词： 硫酸; 催化; 炔丙醇; 亲核取代

本文引用格式

张顺吉 , 刘会丽 . 硫酸催化的炔丙醇快速亲核取代反应[J]. 有机化学, 2020 , 40(5) : 1257 -1265 . DOI: 10.6023/cjoc201911036

Abstract

Sulfuric acid efficiently catalyzes the direct substitution of the hydroxyl group of propargylic alcohols with a variety of C- and O-based nucleophiles to aid C-C and C-O bond formation. The reactions can be performed in an undried solvent under air atmosphere to obtain the desired products in good yields. In most cases, the reaction proceeds to completion in 1 min at room temperature.

Key words： sulfuric acid; catalyzed; propargyl alcohols; nucleophilic substitution

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