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DOI: 10.1055/s-0032-1317162
Tetrabutylammonium Hydrogen Sulfate
Publication History
Publication Date:
09 August 2012 (online)
Introduction
Tetrabutylammonium hydrogen sulfate (TBAHS, 1), is a stable, hygroscopic, white solid (mp 169–171 °C). It is widely used in various fields of chemistry as phase-transfer catalyst (PTC) and ion-pairing reagent as mobile phase additive in HPLC. It has been also used in a variety of organic transformations some of which include the syntheses of triarylpyridines,[ 1 ] N-monosubstituted α-keto amides,[ 2 ] cyclic and acyclic β-disubstituted, α,β-unsaturated ketones,[ 3 ] 3-alkylated indoles,[ 4 ] benzopyran-annulated pyrano[2,3-c]pyrazoles,[ 5 ] N1-alkylated 3,4-dihydropyrimidine-2(1H)-ones,[ 6 ] 2-O-deacetylated glucosyl hydroxamates,[ 7 ] 1,2,3-triazoles,[ 8 ] 1,8-dioxooctahydroxanthenes,[ 9 ] β- and γ-amino ethers, morpholines and their higher homologues,[ 10 ] etc.
Although TBAHS is commercially available and inexpensive, it can be prepared from tetrabutylammonium azide[ 11 ] by treating it with potassium hydrogen sulfate and 10% aqueous sulfuric acid in aqueous medium (Scheme [1], eq. 1) or from tetrabutylammonium thiocyanate[ 12 ] by treating it with relatively concentrated sulfuric acid (70%) at 75 °C (Scheme [1], eq. 2).
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References
- 1 Reddy KS, Reddy RB, Mukkanti K, Thota G, Srinivasulu G. Rasayan J. Chem. 2011; 4: 299
- 2 Shao J, Huang X, Wang S, Liu B, Xu B. Tetrahedron 2012; 68: 573
- 3 Uyanik M, Fukatsu R, Ishihara K. Org. Lett. 2009; 11: 3470
- 4 Damodiran M, Kumar RS, Sivakumar PM, Doble M, Perumal PT. J. Chem. Sci. 2009; 121: 65
- 5 Parmar NJ, Teraiya SB, Patel RA, Talpada NP. Tetrahedron Lett. 2011; 52: 2853
- 6 Singh K, Arora D, Poremsky E, Lowery J, Moreland RS. Eur. J. Med. Chem. 2009; 44: 1997
- 7 Thomas M, Gesson J.-P, Papot S. J. Org. Chem. 2007; 72: 4262
- 8 Singh N, Pandey SK, Tripathi RP. Carbohydr. Res. 2010; 345: 1641
- 9 Karade HN, Sathe M, Kaushik MP. ARKIVOC 2007; (xiii): 252
- 10 Ghorai MK, Shukla D, Bhattacharyya A. J. Org. Chem. 2012; 77: 3740
- 11 De Giorgi M, Landini D, Maia A, Penso M. Synth. Commun. 1987; 17: 521
- 12 Dehmlow EV, Vehre B, Broda W. Synthesis 1985; 508