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DOI: 10.1055/s-2003-41469
Silica Sulfuric Acid: An Efficient Catalyst for the Direct Conversion of Primary and Secondary Trimethylsilyl Ethers to their Corresponding Ethers under Mild and Heterogeneous Conditions
Publication History
Publication Date:
19 September 2003 (online)
Abstract
Primary and secondary trimethylsilyl ethers were converted to their corresponding ethers in the presence silica sulfuric acid with good to excellent yields under mild and heterogeneous conditions.
Keywords
silica sulfuric acid - silyl ethers - ethers - heterogeneous conditions
- 1
Quach TD.Batey RA. Org. Lett. 2003, 5: 1381 - 2
Buck E.Song ZJ.Tschaen D.Dormer PG.Valante RP.Reider PJ. Org. Lett. 2002, 4: 1623 - 3
Busch-Petersen J.Corey EJ. Org. Lett. 2000, 2: 1641 - 4
Xiao XY.Li R.Hurst D.Zhuang H.Shuhao S.Czarnik AW.Robichaud AJ.Wacker DA.Robertson DW. J. Comb. Chem. 2002, 4: 536 - 5
Wang S.Guin JA. Chem. Commun. 2000, 2499 - 6
Bagnell L.Cablewski T.Strauss CR. Chem. Commun. 1999, 283 - 7
Lu B.Li LJ.Li TS.Li JT. J. Chem. Res., Synop. 1998, 604 - 8
Verhoef MJ.Creyghton EJ.Peters JA.Bekkum HV. Chem. Commun. 1997, 1989 - 9
Streitwieser A.Heathcock CH.Kosower EM. Introduction to Organic Chemistry 4th ed.: Macmillan Publishing Company; New York: 1992. p.233 -
10a
Zolfigol MA. Tetrahedron 2001, 57: 9509 -
10b
Mirjalili BF.Zolfigol MA.Bamoniri A. J. Korean Chem. Soc. 2001, 45: 546 -
10c
Zolfigol MA.Bamoniri A. Synlett 2002, 1621 -
10d
Mirjalili BF.Zolfigol MA.Bamoniri A. Molecules 2002, 7: 751 -
10e
Zolfigol MA.Ghaemi E.Madrakian E. Molecules 2002, 7: 734 -
10f
Zolfigol MA.Shirini F.Ghorbani-Choghamarani A.Mohammadpoor-Baltork I. Green Chem. 2002, 4: 562 -
10g
Salehi P.Dabiri M.Zolfigol MA.Bodaghi-fard MA. Tetrahedron Lett. 2003, 44: 2889 -
10h
Zolfigol MA.Chehardoli GA.Mallakpour SE. Synth. Commun. 2003, 33: 833 -
10i
Mirjalili BF.Zolfigol MA.Bamoniri A.Zarei A. Bull. Korean Chem. Soc. 2003, 24: 400 - 13
Firouzabadi H.Karimi B. Synth. Commun. 1993, 23: 1633 - 14
Clark JH. Acc. Chem. Res. 2002, 35: 791
References
Chemicals were purchased from Fluka, Merck and Aldrich chemicals companies. The products were characterized by comparison of their spectral (IR, 1H NMR), TLC and physical data with the authentic samples. Silica sulfuric acid was synthesized according to the our previously reported procedure. [10a] All silyl ethers were synthesized according to the reported procedure. [13]
12Preparation of Silica Sulfuric Acid: A 500 mL suction flask was used. It was equipped with a constant-pressure dropping funnel containing chlorosulfonic acid (23.3 g, 0.2 mol) and gas inlet tube for conducting HCl gas over an adsorbing solution i. e. H2O. Into it were charged 60.0 g of silica gel. Chlorosulfonic acid was added dropwise over a period of 30 min at r.t. HCl gas evolved from the reaction vessel immediately. After the addition was complete the mixture was shaken for 30 min. A white solid (silica sulfuric acid) 76.0 g was obtained. [10a]