2011
DOI: 10.1080/00397911.2010.537424
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Efficient and Novel Method for Thiocyanation of Aromatic Compounds Using Trichloroisocyanuric Acid/Ammonium Thiocyanate/Wet SiO2

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Cited by 33 publications
(11 citation statements)
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“…Nitrogen occurs in all living organisms, primarily in amino acids and thus in proteins and in the nucleic acids (DNA and RNA). [5] Several methods have been explored for the thiocyanation of (hetero)aromatic systems using various reagents such as oxone/NH 4 SCN, [6] N-thiocyanosuccinimde, [7] FeCl 3 /NH 4 SCN, [8] cerric ammonium nitrate (CAN)/NH 4 SCN, [9] montmorillonite K-10 clay/NH 4 SCN, [10] poly(4-diacetoxyiodo)styrene (PDAIS)/NH 4 SCN, [11] acidic Al 2 O 3 /NH 4 SCN, [12] HCl/H 2 O 2 /KSCN, [13] trichloroisocyanuric acid (TCCA)/NH 4 SCN/wet SiO 2 , [14] and citric acid/KSCN/H 2 O 2 . [15] Although the reported 2 K. Nikoofar and S. Gorji methods are efficient, some of them have disadvantages including low yields, strongly oxidizing conditions, long reaction times, high temperatures and use of expensive and toxic reagent or solvent.…”
Section: Introductionmentioning
confidence: 99%
“…Nitrogen occurs in all living organisms, primarily in amino acids and thus in proteins and in the nucleic acids (DNA and RNA). [5] Several methods have been explored for the thiocyanation of (hetero)aromatic systems using various reagents such as oxone/NH 4 SCN, [6] N-thiocyanosuccinimde, [7] FeCl 3 /NH 4 SCN, [8] cerric ammonium nitrate (CAN)/NH 4 SCN, [9] montmorillonite K-10 clay/NH 4 SCN, [10] poly(4-diacetoxyiodo)styrene (PDAIS)/NH 4 SCN, [11] acidic Al 2 O 3 /NH 4 SCN, [12] HCl/H 2 O 2 /KSCN, [13] trichloroisocyanuric acid (TCCA)/NH 4 SCN/wet SiO 2 , [14] and citric acid/KSCN/H 2 O 2 . [15] Although the reported 2 K. Nikoofar and S. Gorji methods are efficient, some of them have disadvantages including low yields, strongly oxidizing conditions, long reaction times, high temperatures and use of expensive and toxic reagent or solvent.…”
Section: Introductionmentioning
confidence: 99%
“…Much effort has been made toward the synthesis of thiocyanates so far. Generally, thiocyanates can be synthesized via the following two major routes (Scheme 1(a)): (1) thiocyanation of organic partners (arenes, organic halides, diazonium salts, and arylboronic acids) in the presence of inorganic thiocyanates 1015 and (2) cyanation of organosulfur compounds including thiols, disulfides, and sulfinates with electrophilic and nucleophilic cyanation reagents. 1620 Thiocyanates can also be prepared via CuCN-mediated direct aerobic oxidative cyanation of thiophenols and diaryl disulfides.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, thiocyanation of aromatic * For correspondence compounds, mononitration and dinitration of phenols have been reported over TCCA/NH 4 SCN/ wet SiO 2 mixture. 10,11 However, based on the literature review, TCCA-functionalized SBA-15 via co-condensation method has not been reported for acylation of indole. Therefore, in the present investigation, our interest emerged to synthesize SBA/TCCA nanocomposites for the first time in the liquid phase acylation of indole.…”
Section: Introductionmentioning
confidence: 99%