메뉴 건너뛰기




Volumn 35, Issue 2, 1996, Pages 422-429

Alkaline condensation of benzotrichloride with 4-alkylphenols as the synthesis method of copper extradants

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINE; CONDENSATION; COPPER; LIQUID/LIQUID EXTRACTION;

EID: 0029673640     PISSN: 08885885     EISSN: None     Source Type: Journal    
DOI: 10.1021/ie950080t     Document Type: Article
Times cited : (3)

References (29)
  • 1
    • 2842615782 scopus 로고    scopus 로고
    • Ultraviolet-absorbing 2-hydroxy-4-phenoxybenzophenone derivatives. German Patent 2146075, 1972
    • Avar, L.; Hofer, K. Ultraviolet-absorbing 2-hydroxy-4-phenoxybenzophenone derivatives. German Patent 2146075, 1972.
    • Avar, L.1    Hofer, K.2
  • 2
    • 2842614615 scopus 로고    scopus 로고
    • Verfahren zur Herstellung von neuen 2-Hydroxybenzophenonen. Swiss Patent 542804, 1973
    • Avar, L.; Hofer, K. Verfahren zur Herstellung von neuen 2-Hydroxybenzophenonen. Swiss Patent 542804, 1973.
    • Avar, L.1    Hofer, K.2
  • 3
    • 23544459211 scopus 로고    scopus 로고
    • Agent for extraction of non-ferrous metal ions. Pol. Patent 112 404, 1978
    • Błaszczak, J.; Szymanowski, J. Agent for extraction of non-ferrous metal ions. Pol. Patent 112 404, 1978.
    • Błaszczak, J.1    Szymanowski, J.2
  • 5
    • 0010287009 scopus 로고
    • Comparison on the Fries and Friedel-Crafts reactions
    • Cullinane, N. M.; Edwards, B. F. Comparison on the Fries and Friedel-Crafts reactions. J. Appl. Chem. 1959, 9, 133-136.
    • (1959) J. Appl. Chem. , vol.9 , pp. 133-136
    • Cullinane, N.M.1    Edwards, B.F.2
  • 6
    • 0006352733 scopus 로고
    • The para Claisen rearrangement: Rearrangement of 6-allyl-2,6-dimethyl-2,4-cyclohexadienone
    • Curtin, D. Y.; Crawford, J. The para Claisen rearrangement: Rearrangement of 6-allyl-2,6-dimethyl-2,4-cyclohexadienone. J. Am. Chem. Soc. 1957, 79, 3156-3159.
    • (1957) J. Am. Chem. Soc. , vol.79 , pp. 3156-3159
    • Curtin, D.Y.1    Crawford, J.2
  • 7
    • 0006374705 scopus 로고
    • An investigation into the importance of heterogenity as a directive influence in the alkylation of sodium 4-tert-butyl-2,6-dimethylphenoxide with benzyl chloride
    • Curtin, D. Y.; Dybvig, D. H. An investigation into the importance of heterogenity as a directive influence in the alkylation of sodium 4-tert-butyl-2,6-dimethylphenoxide with benzyl chloride. J. Am. Chem. Soc. 1962, 84, 225-232.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 225-232
    • Curtin, D.Y.1    Dybvig, D.H.2
  • 8
    • 0001246814 scopus 로고
    • Factors controlling position of alkylation of alkali metal salts of phenols, benzyl and allyl halides
    • Curtin, D. Y.; Crawford, J.; Wilhelm, M. Factors controlling position of alkylation of alkali metal salts of phenols, benzyl and allyl halides. J. Am. Chem. Soc. 1958, 80, 1391-1397.
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 1391-1397
    • Curtin, D.Y.1    Crawford, J.2    Wilhelm, M.3
  • 9
    • 2842581315 scopus 로고
    • Nuclear alkylation of salts of naphthols and anthranol
    • Curtin, D. Y.; Tuites, R. C.; Dybvig, D. H. Nuclear alkylation of salts of naphthols and anthranol. J. Org. Chem. 1960, 25, 155-58.
    • (1960) J. Org. Chem. , vol.25 , pp. 155-158
    • Curtin, D.Y.1    Tuites, R.C.2    Dybvig, D.H.3
  • 10
    • 0345178634 scopus 로고
    • Beziehungen zwischen Struktur und Reaktivitat ambifunktioneller nucleophiler Verbindungen
    • Gompper, R. Beziehungen zwischen Struktur und Reaktivitat ambifunktioneller nucleophiler Verbindungen, Angew. Chem. 1964, 76, 412-423.
    • (1964) Angew. Chem. , vol.76 , pp. 412-423
    • Gompper, R.1
  • 11
    • 84981751296 scopus 로고
    • Ueber die Einwirkung von Methylchloroforr und Phenylchloroform auf alkalische Phenollösungen
    • Heiber, F. Ueber die Einwirkung von Methylchloroforr und Phenylchloroform auf alkalische Phenollösungen, Ber. Dtsch. Chem. Ges. 1891, 24, 3677-3687.
    • (1891) Ber. Dtsch. Chem. Ges. , vol.24 , pp. 3677-3687
    • Heiber, F.1
  • 12
    • 33947468737 scopus 로고
    • Heterogenity as a factor in the alkylation of ambident anions: Peroxide ions
    • Kornblum, N.; Lurie, A. P. Heterogenity as a factor in the alkylation of ambident anions: Peroxide ions. J. Am. Chem. Soc. 1959, 81, 2705-2715.
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 2705-2715
    • Kornblum, N.1    Lurie, A.P.2
  • 13
    • 33947480401 scopus 로고
    • Chemical effects arising from selective solvation: Selective solvation as a factor in the alkylation of ambident anions
    • Kornblum, N.; Berrigan, P. J.; Le Noble, W. J. Chemical effects arising from selective solvation: Selective solvation as a factor in the alkylation of ambident anions. J. Am. Chem. Soc. 1960, 82, 1257-1258.
    • (1960) J. Am. Chem. Soc. , vol.82 , pp. 1257-1258
    • Kornblum, N.1    Berrigan, P.J.2    Le Noble, W.J.3
  • 14
    • 0001100416 scopus 로고
    • Solvation as a factor in the alkylation of ambident anions:The importance of the dielectric factor
    • Kornblum, N.; Seltzer, R.; Haberfield, P. Solvation as a factor in the alkylation of ambident anions:The importance of the dielectric factor. J. Am. Chem. Soc. 1963a, 85, 1148-1154.
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 1148-1154
    • Kornblum, N.1    Seltzer, R.2    Haberfield, P.3
  • 15
    • 33947485234 scopus 로고
    • Solvation as a factor in the alkylation of ambident anions: The importance of the hydrogen bonding capacity of the solvent
    • Kornblum, N.; Berrigan, P. J.; Le Noble, W. J. Solvation as a factor in the alkylation of ambident anions: The importance of the hydrogen bonding capacity of the solvent. J. Am. Chem. Soc. 1963b, 85, 1141-1147.
    • (1963) J. Am. Chem. Soc. , vol.85 , pp. 1141-1147
    • Kornblum, N.1    Berrigan, P.J.2    Le Noble, W.J.3
  • 16
    • 2842516709 scopus 로고    scopus 로고
    • Substituted aromatic ketones. U.K. Patent 1060855, 1967
    • Mather, J. Substituted aromatic ketones. U.K. Patent 1060855, 1967.
    • Mather, J.1
  • 17
    • 2842543586 scopus 로고
    • Aluminium chloride-catalyzed reactions of benzotriehloride with p-cresol
    • Newman, M. S.; Pinkus, A. G. Aluminium chloride-catalyzed reactions of benzotriehloride with p-cresol. J. Org. Chem. 1954a, 19, 985-991.
    • (1954) J. Org. Chem. , vol.19 , pp. 985-991
    • Newman, M.S.1    Pinkus, A.G.2
  • 18
  • 19
    • 2842605710 scopus 로고
    • Aluminium chloride-catalyzed reactions of chlorinated benzotrichlorides with p-cresol
    • Newman, M. S.; Pinkus, A. G. Aluminium chloride-catalyzed reactions of chlorinated benzotrichlorides with p-cresol. J. Org. Chem. 1954c, 19, 996-1001.
    • (1954) J. Org. Chem. , vol.19 , pp. 996-1001
    • Newman, M.S.1    Pinkus, A.G.2
  • 21
    • 0343932482 scopus 로고
    • Alkaline condensation of benzotrichloride with bromophenols
    • Olszanowski, A. Alkaline condensation of benzotrichloride with bromophenols. J. Prakt. Chem. 1990, 332, 1093-1098.
    • (1990) J. Prakt. Chem. , vol.332 , pp. 1093-1098
    • Olszanowski, A.1
  • 22
    • 0343932483 scopus 로고
    • Reaction of benzotrichloride with chlorophenols in alkaline solutions
    • Olszanowski, A. Reaction of benzotrichloride with chlorophenols in alkaline solutions. Pol. J. Chem. 1991, 65, 57-61.
    • (1991) Pol. J. Chem. , vol.65 , pp. 57-61
    • Olszanowski, A.1
  • 23
    • 2842609090 scopus 로고
    • Large laboratory scale synthesis of 2-hydroxy-5-nonylbenzophenone
    • in Polish
    • Olszanowski, A.; Wisniewski, M.; Szymanowski, J. Large laboratory scale synthesis of 2-hydroxy-5-nonylbenzophenone. Chem. Stosow. 1986a, 30, 439-446 (in Polish).
    • (1986) Chem. Stosow. , vol.30 , pp. 439-446
    • Olszanowski, A.1    Wisniewski, M.2    Szymanowski, J.3
  • 24
    • 2842551303 scopus 로고    scopus 로고
    • Method of synthesis agent for preparation hydrophobic solutions for extracting non-ferrous metal ions. Pol. Patent 132840, 1986b (in Polish)
    • Olszanowski, A.; Wisniewski, M.; Szymanowski, J.; Lukowski, A. Method of synthesis agent for preparation hydrophobic solutions for extracting non-ferrous metal ions. Pol. Patent 132840, 1986b (in Polish).
    • Olszanowski, A.1    Wisniewski, M.2    Szymanowski, J.3    Lukowski, A.4
  • 25
    • 0028461535 scopus 로고
    • Synthesis, characterization and performance studies of 2-hydroxy-5-nonylbenzophenone (E)-oxime
    • Sarangi, C.; Rao, Y. R. Synthesis, characterization and performance studies of 2-hydroxy-5-nonylbenzophenone (E)-oxime. Ind. Eng. Chem. Res. 1994, 33, 1665-1668.
    • (1994) Ind. Eng. Chem. Res. , vol.33 , pp. 1665-1668
    • Sarangi, C.1    Rao, Y.R.2
  • 27
    • 2842552386 scopus 로고
    • Synthesis of 2-hydroxy-5-alkylbenzophenone by alkaline condensation of p-alkylphenol with benzotrichloride in the presence of sodium hydroxide
    • in Polish
    • Szymanowski, J.; Blaszczak, J. Synthesis of 2-hydroxy-5-alkylbenzophenone by alkaline condensation of p-alkylphenol with benzotrichloride in the presence of sodium hydroxide. Chem. Stosow. 1982, 26, 99-109 (in Polish).
    • (1982) Chem. Stosow. , vol.26 , pp. 99-109
    • Szymanowski, J.1    Blaszczak, J.2
  • 28
    • 0024029768 scopus 로고
    • Interfacial activity of model 2-hydroxy-5-alkylbenzophenone oximes and their intermediates
    • Szymanowski, J.; Prochaska, K., Interfacial activity of model 2-hydroxy-5-alkylbenzophenone oximes and their intermediates. J. Colloid Interface Sci. 1988, 123, 456-465.
    • (1988) J. Colloid Interface Sci. , vol.123 , pp. 456-465
    • Szymanowski, J.1    Prochaska, K.2
  • 29
    • 0019637899 scopus 로고
    • Production of 2-hydroxy-5-nonylbenzophenone oxime
    • in Polish
    • Szymanowski, J.; Blaszczak, J.; Lukowski, A.; Alejski, K. Production of 2-hydroxy-5-nonylbenzophenone oxime. Przem. Chem. 1981, 60, 533-536 (in Polish).
    • (1981) Przem. Chem. , vol.60 , pp. 533-536
    • Szymanowski, J.1    Blaszczak, J.2    Lukowski, A.3    Alejski, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.