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DOI: 10.1055/s-2006-958948
Perchloric Acid Adsorbed on Silica Gel (HClO4-SiO2) as an Inexpensive, Extremely Efficient, and Reusable Dual Catalyst System for Acetal/Ketal Formation and Their Deprotection to Aldehydes/Ketones
Publication History
Publication Date:
14 December 2006 (online)

Abstract
Perchloric acid adsorbed on silica gel (HClO4-SiO2) is reported as extremely efficient, inexpensive, and reusable catalyst for dual role for protection of aldehydes/ketones (with trialkyl orthoformates) as acetals/ketals and deprotection (with water-alcohol) to regenerate the carbonyl compounds in high yields at room temperature and in short times. Acetalization/ketalization of electrophilic aldehydes/ketones was carried out under solvent-free conditions. Weakly electrophilic aldehydes/ketones and aldehydes having a substituent that can coordinate with the catalyst, required the corresponding alcohol as solvent.
Key words
acetals - ketals - aldehydes - ketones - trimethyl orthoformate (TMOF) - triethyl orthoformate (TEOF) - protection/deprotection - HClO4-SiO2 - dual catalyst
- 1
Carey JS.Laffan D.Thomson C.Williams MT. Org. Biomol. Chem. 2006, 4: 2337MissingFormLabel - 2a
Meskens FAJ. Synthesis 1981, 501 - 2b
Greene TW.Wuts PGM. Protecting Groups in Organic Synthesis 3rd ed.: Wiley; New York: 1999. - 3a I2:
Basu MK.Samajdar S.Becker FF.Banik BK. Synlett 2002, 319 - 3b COCl2:
Velusamy S.Punniyamurthy T. Tetrahedron Lett. 2004, 45: 4917 - 3c RuCl3:
De S K.Gibbs RA. Tetrahedron Lett. 2004, 45: 8141 - 3d SO3H-SiO2:
Shimizu K.Hayashi E.Hatamachi T.Kodama T.Kitayama Y. Tetrahedron Lett. 2004, 45: 5138 - 3e [Hmim]BF4:
Wu H.-H.Yang FY.Cui P.Tang J.He M.-Y. Tetrahedron Lett. 2004, 45: 4963 - 3f CAN-Na2CO3:
Nair V.Rajan R.Balagopal L.Nair LG.Ros S.Mohanan K. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 2005, 44: 141 - 3g Clays and zeolites:
Thomas B.Prathapan S.Sugunan S. Micropor. Mesopor. Mat. 2005, 80: 65 - 3h Polymer-supported acid catalysts in an electroosmotic flow reactor:
Wiles C.Watts P.Haswell SJ. Tetrahedron 2005, 61: 5209 - 4a ZrCl4:
Firouzabadi H.Iranpoor N.Karimi B. Synlett 1999, 321 - 4b NBS:
Karimi B.Seradj H.Ebrahimian G.-R. Synlett 1999, 1456 - 4c TBATB:
Gopinath R.Haque SJ.Patel BK. J. Org. Chem. 2002, 67: 5842 - 4d B10H14:
Lee SH.Lee JH.Yoon CM. Tetrahedron Lett. 2002, 43: 2699 - 4e LiBF4:
Hamada N.Kazahaya K.Shimizu H.Sato T. Synlett 2004, 1074 - 4f InCl3:
Ranu BC.Jana R.Samanta S. Adv. Synth. Catal. 2004, 346: 446 - 4g Cu(BF4)2:
Kumar R.Chakraborti AK. Tetrahedron Lett. 2005, 46: 8319 - 5 Olah G. A., Prakash G. K. S.; Superacids; Wiley: New York, 1985;
MissingFormLabel
- 6a Bi(OTf)3:
Leonard NM.Oswald MC.Freiberg DA.Nattier BA.Smith RC.Mohan RS. J. Org. Chem. 2002, 67: 5202 - 6b TMSOTf-(CH2OTMS)2:
Hwu JR.Leu L.-C.Robl JA.Anderson DA.John MW. J. Org. Chem. 1987, 52: 188 - 6c TMSOTf-(CH2OTMS)2:
Hwu JR.John MW. J. Org. Chem. 1985, 50: 3946 - 7
Dumeunier R.Markó IE. Tetrahedron Lett. 2004, 45: 825 - 8
Orita A.Tanahashi C.Kakuda A.Otera J. J. Org. Chem. 2001, 66: 8926 - 9
Qian C.Huang T. J. Org. Chem. 1998, 63: 4125 - 10
Répichet S.Zwick A.Vendier L.Roux CL.Dubac J. Tetrahedron Lett. 2002, 43: 993 - 11
Ishihara K.Karumi Y.Kubota M.Yamamoto H. Synlett 1990, 839 - 12
Foropoulos J.DesMarteau DD. Inorg. Chem. 1984, 23: 3720 - 13
Chakraborti AK. . J. Org. Chem. 2006, 71: 5785 ; and references cited therein - 14
Ishihara K.Kubota M.Yamamoto H. Synlett 1996, 265 - 15a
Garg SK.Kumar R.Chakraborti AK. Tetrahedron Lett. 2005, 46: 1721 - 15b
Garg SK.Kumar R.Chakraborti AK. Synlett 2005, 1370 - 15c
Chakraborti AK.Sharma L.Gulhane R. . Tetrahedron 2003, 59: 7661 - 15d
Chakraborti AK.Gulhane R. . Synlett 2003, 1805 - 15e
Chakraborti AK.Bhagat S.Rudrawar S. Tetrahedron Lett. 2004, 45: 7641 - 15f
Kumar R.Thilagavathi R.Gulhane R.Chakraborti AK. J. Mol. Catal. A: Chem. 2006, 250: 227 - 15g
.
Chakraborti AK. J. Mol. Catal. A: Chem. 2006, in press - 16
Bartoli G.Bosco M.Dalpozzo R.Marcantoni E.Massaccesi M.Rinaldi S.Sambri L. Synlett 2003, 39 - HClO4-SiO2 is not commercially available and was first prepared and used by Chakraborti et al.:
- 17a
Chakraborti AK.Gulhane R. Chem. Commun. 2003, 1896 - 17b
Chakraborti AK, andGulhane R. inventors; Indian Patent 266/DEL. - Other uses:
- 17c
Agarwal A.Rani S.Vankar YD. J. Org. Chem. 2004, 69: 6137 - 17d
Misra AK.Tiwari P.Madhusudan SK. Carbohydr. Res. 2005, 340: 325 - 17e
Mukhopadhyay B.Russell DA.Field RA. Carbohydr. Res. 2005, 340: 1075 - 17f
Khan AT.Parvin T.Choudhury LK. Synthesis 2006, 2497 - 17g
Das B.Venkateswarlu K.Majhi A.Reddy MR.Reddy KN.Rao YK.Ravikumar K.Sridhar B. J. Mol. Catal. A: Chem. 2006, 246: 276 - 17h
Khan AT.Ghosh S.Choudhury LH. Eur. J. Org. Chem. 2006, 2226 - 17i
Rudrawar S.Besra RC.Chakraborti AK. Synthesis 2006, 2767 - 17j
Chakraborti AK.Sunay V.Chankeshwara SV. Org. Biomol. Chem. 2006, 4: 2769 - 18a I2 in acetone:
Sun J.Dong Y.Cao L.Wang X.Wang S.Hu Y. J. Org. Chem. 2004, 69: 8932 - 18b H2O at 453 K and 1.02 MPa:
Sato K.Kishimoto T.Morimoto M.Saimoto H.Shigemasa Y. Tetrahedron Lett. 2003, 44: 8623 - 18c Er(OTf)3:
Dalpozzo R.De Nino A.Maiuolo L.Nardi M.Procopio A.Tagarelli A. Synthesis 2004, 296 - 18d CAN:
Ates A.Gautier A.Leroy B.Plancher J.-M.Quesnel Y.Vanherck J.-C.Markó IE. Tetrahedron 2003, 59: 8989 - 18e β-CD:
Krishnaveni NS.Surendra K.Reddy MA.Nageswar YVD.Rama Rao K. J. Org. Chem. 2003, 68: 2018 - 18f Ce(OTf)3:
Dalpozzo R.De Nino A.Maiuolo L.Procopio A.Tagarelli A.Sindona G.Bartoli G. J. Org. Chem. 2002, 67: 9093 - 18g Peroxymonosulfate on alumina:
Bose DS.Jayalakshmi B.Narsaiah AV. Synthesis 2000, 67 - 19
Tundo P.Anastas P.Black DS.Breen J.Collins T.Memoli S.Miyamoto J.Polyakoff M.Tumas W. Pure Appl. Chem. 2000, 72: 1207