Room Temperature Ionic Liqiuds-New Choline Derivatives

• Autorzy: Pernak J. , Chwała P. , Syguda A.
• Języki publikacji: EN

Abstrakty

EN

New room temperature ionic liquids - choline derivatives were prepared by Menschutkin reaction with alkyl chloromethyl ethers and anion changed to bis(trifluoromethylsulfonyl) amide ion. The newly obtained butoxymethyl(2-hydroxyethyl)dimethylammonium bis(trifluoromethanesulfonyl)amide was successfully tested as a solvent for O-acylation in two-phase reaction system. The ionic liquid-catalyst system was recycled and reused.

Słowa kluczowe

EN

room temperature ionic liquid; choline derivatives; phase-transfer catalysis

• Wydawca: Polskie Towarzystwo Chemiczne
• Czasopismo: Polish Journal of Chemistry
• Rocznik: 2004
• Tom: Vol. 78 / nr 4
• Strony: 539--546
• Opis fizyczny: Bibliogr. 24 poz., rys.

Twórcy

autor

Pernak J.

• Poznań University of Technology, Faculty of Chemical Technology, pl. M. Skołodowskiej-Curie 2, 60-965 Poznań, Poland

autor

Chwała P.

• Poznań University of Technology, Faculty of Chemical Technology, pl. M. Skołodowskiej-Curie 2, 60-965 Poznań, Poland

autor

Syguda A.

• Poznań University of Technology, Faculty of Chemical Technology, pl. M. Skołodowskiej-Curie 2, 60-965 Poznań, Poland

Bibliografia

• 1. Welton T., Chem. Rev., 99, 2071 (1999).
• 2. Wasserscheid P. and Keim W., Angew. Chem. Int. Ed. Engl., 39, 3772 (2000).
• 3. Sheldon R., Chem. Commun., 2399 (2001).
• 4. Olivier-Bourbigou H. and Magna L., J. Mol. Catal. A: Chem., 182-183,419 (2002).
• 5. Dupont J., de Souza R.F. and Suarez P.A.Z., Chem. Rev., 102, 3667 (2002).
• 6. Wasserscheid P. and Welton T., Ionic Liquids in Synthesis. John Wiley & Sons, NY 2002.
• 7. Wasserscheid P., BOsmann A. and Bolm C., Chem. Comm., 200 (2002).
• 8. Abbott A.P., Capper G., Davies D.L., Munro H.L. and Tambyrajah V., Chem. Comm., 2010 (2001).
• 9. Lygo B., Crosby J. and Peterson J.A., Tetrahedron Lett., 40, 1385 (1999).
• 10. Ooi T., Kameda M. and Maruoka K., J. Am. Chem. Soc., 121, 6519 (1999).
• 11. Kim D.Y., Huh S.C. and Kim S.M., Tetrahedron Lett., 42, 6299 (2001).
• 12. Chinchilla R., Mazon P. and Najera C., Tetrahedron Asymmetry, 13, 927 (2002).
• 13. Fannin Jr. A.A., King L.A., Levisky J.A. and Wilkes J.S., J. Phys. Chem., 88, 2609 (1984).
• 14. Huddleston J.G., Visser A.E., Reichert M., Willauer H.D., Broker G.A. and Rogers R.D., Green Chemistry, 3, 156 (2001).
• 15. Pemak J., Czepukowicz A. and Pozniak R., Ind. Eng. Chem. Res., 40,2379 (2001).
• 16. Pemak J., OIsz6wka A. and Olszewski R, Polish J. Chem., 77,179 (2003).
• 17. Pemak J. and Goc I., Polish J. Chem., 77, 975 (2003).
• 18. Aggarwal A., Lancaster N.L., Sethi A.R and WeltonT., Green Chemistry, 4, 517 (2002).
• 19. Holbrey J.D. and Seddon K.R., J. Chem. Soc., Dalton Trans., 2133 (1999).
• 20. Eynde J.J.V. and Mailleux I., Synthetic Commun., 31, 1 (2001).
• 21. Deng Y., Shi F., Beng J. and Qiao K., J. Mol. Catal. A-Chem., 165, 33 (2001).
• 22. Fraga-Dubreuil J., Bourahla K., Rahmouni M., Bazureau J. P. and Hamelin J., Catalysis Commun., 3, 185 (2002).
• 23. Brinchi L., Germani R. and Savelli G., Tetrahedron Lett., 44, 2027 (2003).
• 24. Szeja W„ Synthesis, 402 (1980).