Solid-Liquid Phase Transfer Catalysis Without Solvent: A Mild and Efficient Preparation of Mono and Di-Ethers Derived from 8-Hydroxyquinoline

References

• Strzelecka , H. and Rivory , J. 1981 . Chem. Scripta , 17 : 95 and quoted references
   Google Scholar
• Lindner , W. , Fugnitto , R. , Strzelecka , H. and Rivory , J. 1984 . Synthetic Metals Vol. 8 , 000
   Google Scholar
• Shchukina , M. H. and Savitskaya , N. V. 1952 . Zhur. Obshchei Khim. , 22 : 1218 J. Gen. Chem. USSR, 22, 1263 1953; of C.A. 47, 7505f 1953
   Google Scholar
• Horclois , R. J. , Gilbert , L. A. and Marcilhacy , D. M.G. 1949 . patents Brit , 626 : 007 US 2,499,661 1950; Fr 1,001,982 1952; of C.A, 51, 7435 1957
   Google Scholar
• Heimann , U. and Vcgtle , F. 1979 . Chem. Ber. , 112 : 3034
   Google Scholar
• Barry , J. , Bram , G. , Decodts , G. , Loupy , A. , Pigeon , P. and Sansoulet , J. 1982 . Tetrahedron Lett. , 23 : 5407
   Google Scholar
• Barry , J. , Bram , G. , Decodts , G. , Loupy , A. , Pigeon , P. and Sansoulet , J. 1983 . Tetrahedron , 39 : 2673
   Web of Science ®Google Scholar
• Barry , J. , Bram , G. , Decodts , G. , Loupy , A. , Pigeon , P. and Sansoulet , J. 1983 . Tetrahedron , 39 : 2669
   Web of Science ®Google Scholar
• Barry , J. , Bram , G. , Decodts , G. , Loupy , A. , Pigeon , P. and Sansoulet , J. Tetrahedron , in the press
   Google Scholar
• Starks , C . 1971 . J. Amer. Chem. Soc. , 93 : 195 Aliquat 336 is essentially constituted of trioctylmethylammonium chlorid
   Web of Science ®Google Scholar
• Ardashev , B. I. and Minkin; , V. I. 1958 . Zhur. Obsch. Khim. , 28 : 545 C.A. 52, 13729d 1958
   Google Scholar
• Buehler , C. A. and Pearson , D. E. 1970 . Survey of Organic Chemistry , 285 – 382 . New York : Wiley Interscience . and quoted references
   Google Scholar
• Johnstone , R. A.W. and Rose , M. E. 1979 . Tetrahedron , 35 : 2169
   Web of Science ®Google Scholar
• Hiratani , K. , Aiba , S. and Nakagawa , T. 1980 . Chem. Lett. , : 477
   Web of Science ®Google Scholar
• Kessar , S. V. , Gupta , Y. P. , Mohammad , T. , Goyal , M. and Kawal , K. S. 1983 . J.C.S. Chem. Comm. , : 400
   Google Scholar
• McKillop , A. , Fiaud , J. C. and Hug , R. P. 1974 . Tetrahedron , 30 : 1379
   Web of Science ®Google Scholar
• Chin-Hsien , M. , Miang-Te , L. and Xiao-Hun , C. 1982 . Synthesis , : 858
   Google Scholar
• We obtained very moderate yields (5-12%) when we tried to prepare the diethers in classical liquid-liquid PTC conditions in the presence of a solvent (CH2Cl2 or C6H6). On the other hand, this technique was successful in the case of very reactive alkylating agents (short chains, allylic, benzylic or activated aromatic halides)15,16
   Google Scholar