H2SO4 catalyzed tandem alkylation-hydrolysis reaction of β-ethylthio-β-indolyl-α, β-unsaturated ketones and alcohols: Feasible synthesis of α-alkylated 3-aroylacetylindoles and 3-arylpropionylindoles
{"title":"H2SO4 catalyzed tandem alkylation-hydrolysis reaction of β-ethylthio-β-indolyl-α, β-unsaturated ketones and alcohols: Feasible synthesis of α-alkylated 3-aroylacetylindoles and 3-arylpropionylindoles","authors":"Tianqi Zhang (Investigation), Xiaobo Zhao (Funding acquisition Supervision), Chunyan Wu (Investigation), Xuexian Zhu (Validation), Helong Bai (Writing – review & editing), Haifeng Yu (Supervision Writing – original draft)","doi":"10.1080/00397911.2026.2733489","DOIUrl":null,"url":null,"abstract":"<div><div>H<sub>2</sub>SO<sub>4</sub> catalyzed tandem alkylation-hydrolysis reaction of <em>β</em>-ethylthio-<em>β</em>-indolyl-<em>α</em>, <em>β</em>-unsaturated ketones and alcohols has been developed to access <em>α</em>-alkylated 3-aroylacetylindoles in up to 90% yield. Subsequent debenzoylation of <em>α</em>-alkylated 3-aroylacetylindoles in the presence of 1.0 equivalent of NaOH provides 3-arylpropionylindoles in excellent yields. The facile accessibility of various valuable <em>α</em>-alkylated 3-aroylacetylindoles and 3-arylpropionylindoles demonstrates the high practicability of this method.</div></div>","PeriodicalId":22119,"journal":{"name":"Synthetic Communications","volume":"56 18","pages":"Pages 1430-1439"},"PeriodicalIF":2.0000,"publicationDate":"2026-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthetic Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S0039791126000871","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/9/29 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
Abstract
H2SO4 catalyzed tandem alkylation-hydrolysis reaction of β-ethylthio-β-indolyl-α, β-unsaturated ketones and alcohols has been developed to access α-alkylated 3-aroylacetylindoles in up to 90% yield. Subsequent debenzoylation of α-alkylated 3-aroylacetylindoles in the presence of 1.0 equivalent of NaOH provides 3-arylpropionylindoles in excellent yields. The facile accessibility of various valuable α-alkylated 3-aroylacetylindoles and 3-arylpropionylindoles demonstrates the high practicability of this method.
期刊介绍:
Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.