2012
DOI: 10.5155/eurjchem.3.4.475-479.709
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Synthesis of bis(indolyl)methanes using molten N-butylpyridinium bromide

Abstract: A simple and rapid protocol has been developed for the synthesis of bis(indolyl)methane compounds in excellent yields using molten N-butyl-pyridinium bromide as a solvent and a working catalyst for the reaction. Synthesis of bis(indolyl)methane compounds were accomplished at moderate experimental conditions of temperature and ambient pressure, also involving an electrophilic substitution reaction of indoles with several aromatic aldehydes. The derivatives were confirmed with mass and other usual spectroscopic … Show more

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Cited by 22 publications
(4 citation statements)
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References 49 publications
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“…[100][101][102][103][104][105][106] An astonishing range of synthetic methods have been utilized to produce bisindolylmethanes (BIMs), which are molecules of interest, the most widely recognized of which is the Friedel-Crafts coupling reaction between aldehydes and indoles. [107][108][109][110][111][112][113] In 2019, Badillo and co-workers reported a highly efficient C-C bond formation strategy using a visible-light-induced thiourea photoacid catalyst (Scheme 19). 114 Photoirradiation of indoles and aldehydes and isatins catalyzed by Schreiner's thiourea [(N,N′-bis[3,5-bis(trifluoromethyl)phenyl]thiourea] (9) resulted in double FC arylation to give triarylmethanes and 3,3′-diarylindolin-2-ones, respectively.…”
Section: Aldehydes and Ketones As Alkylating Agentsmentioning
confidence: 99%
“…[100][101][102][103][104][105][106] An astonishing range of synthetic methods have been utilized to produce bisindolylmethanes (BIMs), which are molecules of interest, the most widely recognized of which is the Friedel-Crafts coupling reaction between aldehydes and indoles. [107][108][109][110][111][112][113] In 2019, Badillo and co-workers reported a highly efficient C-C bond formation strategy using a visible-light-induced thiourea photoacid catalyst (Scheme 19). 114 Photoirradiation of indoles and aldehydes and isatins catalyzed by Schreiner's thiourea [(N,N′-bis[3,5-bis(trifluoromethyl)phenyl]thiourea] (9) resulted in double FC arylation to give triarylmethanes and 3,3′-diarylindolin-2-ones, respectively.…”
Section: Aldehydes and Ketones As Alkylating Agentsmentioning
confidence: 99%
“…ILs are supposed to be considered as supramolecular materials and provide a broad spectrum of applications, such as green medium for organic reactions, electrolytes for solar and fuel cells, heat transfer fluids in nuclear reactors, in dissolution of cellulose, etc. [6][7][8]. The versatility of these molecules is attributed to their exceptional structural behaviour in vapour and solution phases [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…Subsequently, Wilkes, one of the co-worker of Osteryoung, performed a systematic study on 1, 3-dialkylimidazolium salts and classified ionic liquids (ILs) from molten salts on the basis of their melting temperature. To date, the huge literature cited on ILs accentuates the importance of these salts in the field of materials [2][3][4][5][6][7][8][9][10]. ILs belong to a class of organic solvents with high polarity and a pre-organized solvent structure, and are categorized as supramolecular solvents after water [11].…”
Section: Introductionmentioning
confidence: 99%