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

IF 2 3区 化学 Q3 CHEMISTRY, ORGANIC
Synthetic Communications Pub Date : 2026-09-17 Epub Date: 2026-09-29 DOI:10.1080/00397911.2026.2733489
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)
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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.
H2SO4催化β-乙基硫-β-吲哚基-α、β-不饱和酮和醇的串联烷基化水解反应:α-烷基化3-芳基乙酰啉和3-芳基丙炔啉的可行合成
利用H2SO4催化β-乙基硫-β-吲哚-α、β-不饱和酮和醇的串联烷基化水解反应,得到了收率高达90%的α-烷基化3-芳基乙酰啉。在1.0当量的NaOH存在下,α-烷基化的3-芳基乙酰林多随后进行去苯甲酰化,得到收率很高的3-芳基丙炔林多。各种有价α-烷基化3-芳基乙酰啉和3-芳基丙炔啉的易得性证明了该方法的实用性。
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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
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.
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