[TMBSPD][OMs]2: An Efficient Recyclable Ionic Liquid for the Synthesis of Bis(indolyl)methanes from Aldehydes or Ketones and Indoles at Ambient Temperature

An efficient synthesis of bis(indolyl)methanes by the reaction of aldehydes and ketones with indoles catalyzed by N,N,N′,N′-tetramethyl-N,N′-bis(sulfo)biphenyl-4,4′-diaminium bis(methanesulfonate) ([TMBSPD][OMs]2) has been developed. The reaction proceeds in ethanol at room temperature to provide the desired products in good to excellent yields. The proposed methodology is characterized by a broad substrate scope, environmental friendliness, and cost efficiency.

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Publication Details

Journal
Russian Journal of Organic Chemistry
Published
2024-10-01
DOI
https://doi.org/10.1134/s1070428024100142
Primary Topic
Synthesis of Indole Derivatives
Type
article
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article

[TMBSPD][OMs]2: An Efficient Recyclable Ionic Liquid for the Synthesis of Bis(indolyl)methanes from Aldehydes or Ketones and Indoles at Ambient Temperature

Farahnaz K. Behbahani, M. Janmohammadi
Russian Journal of Organic Chemistry
Synthesis of Indole Derivatives
article

[TMBSPD][OMs]2: An Efficient Recyclable Ionic Liquid for the Synthesis of Bis(indolyl)methanes from Aldehydes or Ketones and Indoles at Ambient Temperature

Farahnaz K. Behbahani, M. Janmohammadi
article en

Abstract

An efficient synthesis of bis(indolyl)methanes by the reaction of aldehydes and ketones with indoles catalyzed by N,N,N′,N′-tetramethyl-N,N′-bis(sulfo)biphenyl-4,4′-diaminium bis(methanesulfonate) ([TMBSPD][OMs]2) has been developed. The reaction proceeds in ethanol at room temperature to provide the desired products in good to excellent yields. The proposed methodology is characterized by a broad substrate scope, environmental friendliness, and cost efficiency.

Russian Journal of Organic ChemistryVol. 60(10)
Islamic Azad University, Karaj (IR)
Openalex Percentile: Top 83%
Synthesis of Indole Derivatives
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