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Volumn 47, Issue 22, 2008, Pages 8631-8638

Esterification of long-chain acids and alcohols catalyzed by ferric chloride hexahydrate

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; CARBOXYLATION; CARBOXYLIC ACIDS; CATALYSIS; CHROMIUM; COPPER; ESTERIFICATION; ESTERS; FATTY ACIDS; HAFNIUM COMPOUNDS; HYDRATES; MANGANESE; MANGANESE COMPOUNDS; NITROGEN COMPOUNDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; SALTS; ZINC;

EID: 57249088655     PISSN: 08885885     EISSN: None     Source Type: Journal    
DOI: 10.1021/ie800957b     Document Type: Article
Times cited : (43)

References (44)
  • 2
    • 33745617665 scopus 로고    scopus 로고
    • Refractive indices, order parameter and principal polarizability of cholesteric liquid crystals and their mixtures
    • Srivastava, A. K.; Monohar, R.; Shukla, J. P. Refractive indices, order parameter and principal polarizability of cholesteric liquid crystals and their mixtures. Mol. Cryst. Liq. Cryst. 2006, 454, 627.
    • (2006) Mol. Cryst. Liq. Cryst , vol.454 , pp. 627
    • Srivastava, A.K.1    Monohar, R.2    Shukla, J.P.3
  • 3
    • 21144444539 scopus 로고    scopus 로고
    • Thermotropic liquid crystalline drugs
    • Bunjes, H.; Rades, T. J. Thermotropic liquid crystalline drugs. J. Pharm. Pharmacol. 2005, 57, 807.
    • (2005) J. Pharm. Pharmacol , vol.57 , pp. 807
    • Bunjes, H.1    Rades, T.J.2
  • 6
    • 0001208710 scopus 로고
    • Trost, R. M, Flemings, I, Eds, Pergamon: Oxford, Chapter 2.3, pp
    • Benz, G. Comprehensive Organic Syntheses; Trost, R. M., Flemings, I., Eds.; Pergamon: Oxford, 1991; Vol. 6, Chapter 2.3, pp 381-417.
    • (1991) Comprehensive Organic Syntheses , vol.6 , pp. 381-417
    • Benz, G.1
  • 9
    • 6444219501 scopus 로고    scopus 로고
    • Esterification of palmitic acid with methanol over tungsten oxide supported on zirconia solid acid catalysts: Effect of method of preparation of the catalyst on its structural stability and reactivity
    • Ramuz, S. N.; Lingaiah, N.; Devi, B. L. A. P.; Prasad, R. B. N.; Suryanarayana, I.; Sai Prasad, P. S. Esterification of palmitic acid with methanol over tungsten oxide supported on zirconia solid acid catalysts: effect of method of preparation of the catalyst on its structural stability and reactivity. Appl. Catal., A: Gen. 2004, 276, 163.
    • (2004) Appl. Catal., A: Gen , vol.276 , pp. 163
    • Ramuz, S.N.1    Lingaiah, N.2    Devi, B.L.A.P.3    Prasad, R.B.N.4    Suryanarayana, I.5    Sai Prasad, P.S.6
  • 10
    • 0345276499 scopus 로고    scopus 로고
    • Highly efficient esterification of carboxylic acids with alcohols by montmorillonite-enwrapped titanium as a heterogeneous acid catalyst
    • Kawabata, T.; Mizugaki, T.; Ebitani, K.; Kaneda, K. Highly efficient esterification of carboxylic acids with alcohols by montmorillonite-enwrapped titanium as a heterogeneous acid catalyst. Tetrahedron Lett. 2003, 44, 9205.
    • (2003) Tetrahedron Lett , vol.44 , pp. 9205
    • Kawabata, T.1    Mizugaki, T.2    Ebitani, K.3    Kaneda, K.4
  • 12
    • 0141457559 scopus 로고    scopus 로고
    • Organosulfonic acid-functionalized mesoporous silicas for the esterification of fatty acid
    • Mbaraka, I.; Radu, D. R.; Lin, V. S.-Y.; Shanks, B. H. Organosulfonic acid-functionalized mesoporous silicas for the esterification of fatty acid. J. Catal. 2003, 219, 329.
    • (2003) J. Catal , vol.219 , pp. 329
    • Mbaraka, I.1    Radu, D.R.2    Lin, V.S.-Y.3    Shanks, B.H.4
  • 13
    • 13444266273 scopus 로고    scopus 로고
    • Design of multifunctionalized mesoporous silicas for esterification of fatty acid
    • Mbaraka, I.; Shanks, B. H. Design of multifunctionalized mesoporous silicas for esterification of fatty acid. J. Catal. 2005, 229, 365.
    • (2005) J. Catal , vol.229 , pp. 365
    • Mbaraka, I.1    Shanks, B.H.2
  • 14
    • 0037048606 scopus 로고    scopus 로고
    • Dehydration reactions in water. Bronsted acid-surfactant-combined catalyst for ester, ether, thioether, and dithioacetal formation in water
    • Chem. Soc
    • Manabe, K.; Iimura, S.; Sun, X.-M.; Kobayashi, S. Dehydration reactions in water. Bronsted acid-surfactant-combined catalyst for ester, ether, thioether, and dithioacetal formation in water. J. Am. Chem. Soc. 2002, 123, 11971.
    • (2002) J. Am , vol.123 , pp. 11971
    • Manabe, K.1    Iimura, S.2    Sun, X.-M.3    Kobayashi, S.4
  • 15
    • 0347418218 scopus 로고    scopus 로고
    • Recyclable and selective Lewis acid catalysts for transesterification and direct esterification in a fluorous biphase system: Tin(IV) and hafnium(IV) bis(perfluorooctanesulfonyl)amide complexes
    • Hao, X.; Yoshida, A.; Nishikido, J. Recyclable and selective Lewis acid catalysts for transesterification and direct esterification in a fluorous biphase system: tin(IV) and hafnium(IV) bis(perfluorooctanesulfonyl)amide complexes. Tetrahedron Lett. 2003, 45, 781.
    • (2003) Tetrahedron Lett , vol.45 , pp. 781
    • Hao, X.1    Yoshida, A.2    Nishikido, J.3
  • 16
    • 8844266155 scopus 로고    scopus 로고
    • Efficient method for the esterification of carboxylic acids with alcohols using di-2-thienyl carbonate promoted by DMAP and iodine
    • Oohashi, Y.; Fukumoto, K.; Mukaiyama, T. Efficient method for the esterification of carboxylic acids with alcohols using di-2-thienyl carbonate promoted by DMAP and iodine. Chem. Lett. 2004, 33, 968.
    • (2004) Chem. Lett , vol.33 , pp. 968
    • Oohashi, Y.1    Fukumoto, K.2    Mukaiyama, T.3
  • 17
    • 0034559421 scopus 로고    scopus 로고
    • Catalyzed or uncatalyzed esterification reaction of oleic acid with 2-ethylhexanol
    • Lacaze-Dufaure, C.; Mouloungui, Z. Catalyzed or uncatalyzed esterification reaction of oleic acid with 2-ethylhexanol. Appl. Catal., A: Gen. 2000, 204, 223.
    • (2000) Appl. Catal., A: Gen , vol.204 , pp. 223
    • Lacaze-Dufaure, C.1    Mouloungui, Z.2
  • 18
    • 0034634399 scopus 로고    scopus 로고
    • Direct condensation of carboxylic acids with alcohols catalyzed by hafhium(IV) salts
    • Ishihara, K.; Ohara, S.; Yamamoto, H. Direct condensation of carboxylic acids with alcohols catalyzed by hafhium(IV) salts. Science 2000, 290, 1140.
    • (2000) Science , vol.290 , pp. 1140
    • Ishihara, K.1    Ohara, S.2    Yamamoto, H.3
  • 19
    • 0034930214 scopus 로고    scopus 로고
    • A green method for the selective esterification of primary alcohols in the presence of secondary alcohols or aromatic alcohols
    • Ishihara, K.; Nakayama, M.; Ohara, S.; Yamamoto, H. A green method for the selective esterification of primary alcohols in the presence of secondary alcohols or aromatic alcohols. Synlett 2001, 1117.
    • (2001) Synlett , pp. 1117
    • Ishihara, K.1    Nakayama, M.2    Ohara, S.3    Yamamoto, H.4
  • 20
    • 0037037934 scopus 로고    scopus 로고
    • Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium(IV) or zirconium(IV) salts
    • Ishihara, K.; Nakayama, M.; Ohara, S.; Yamamoto, H. Direct ester condensation from a 1:1 mixture of carboxylic acids and alcohols catalyzed by hafnium(IV) or zirconium(IV) salts. Tetrahedron 2001, 58, 8179.
    • (2001) Tetrahedron , vol.58 , pp. 8179
    • Ishihara, K.1    Nakayama, M.2    Ohara, S.3    Yamamoto, H.4
  • 21
    • 7044239414 scopus 로고    scopus 로고
    • Water-tolerant and reusable catalysts for direct ester condensation between equimolar amounts of carboxylic acids and alcohols
    • Nakayama, M.; Sato, A.; Ishihara, K.; Yamamoto, H. Water-tolerant and reusable catalysts for direct ester condensation between equimolar amounts of carboxylic acids and alcohols. Adv. Synth. Catal. 2004, 346, 1275.
    • (2004) Adv. Synth. Catal , vol.346 , pp. 1275
    • Nakayama, M.1    Sato, A.2    Ishihara, K.3    Yamamoto, H.4
  • 22
    • 24644458677 scopus 로고    scopus 로고
    • Zr(IV)Fe(III), Ga(III), and Sn(IV) binary metal complexes as synergistic and reusable esterification catalysts
    • Sato, A.; Nakamura, Y.; Maki, T.; Ishihara, K.; Yamamoto, H. Zr(IV)Fe(III), Ga(III), and Sn(IV) binary metal complexes as synergistic and reusable esterification catalysts. Adv. Synth. Catal. 2005, 347, 1337.
    • (2005) Adv. Synth. Catal , vol.347 , pp. 1337
    • Sato, A.1    Nakamura, Y.2    Maki, T.3    Ishihara, K.4    Yamamoto, H.5
  • 23
    • 33748270464 scopus 로고    scopus 로고
    • Iron(III)-Zirconium(IV) combined salt immobilized on AHpolystyrylbutyl) pyridinium triflylimide as a reusable catalyst for a dehydrative esterification reaction
    • Nakamura, Y.; Maki, T.; Wang, X.; Ishihara, K.; Yamamoto, H. Iron(III)-Zirconium(IV) combined salt immobilized on AHpolystyrylbutyl) pyridinium triflylimide as a reusable catalyst for a dehydrative esterification reaction. Adv. Synth. Catal. 2006, 348, 1505.
    • (2006) Adv. Synth. Catal , vol.348 , pp. 1505
    • Nakamura, Y.1    Maki, T.2    Wang, X.3    Ishihara, K.4    Yamamoto, H.5
  • 24
    • 27644524570 scopus 로고    scopus 로고
    • N-Alkyl-4-boronopyridinium halides versus boric acid as catalysts for the esterification of α-hydroxy- carboxylic acids
    • Maki, T.; Ishihara, K.; Yamamoto, H. N-Alkyl-4-boronopyridinium halides versus boric acid as catalysts for the esterification of α-hydroxy- carboxylic acids. Org. Lett. 2005, 7, 5047.
    • (2005) Org. Lett , vol.7 , pp. 5047
    • Maki, T.1    Ishihara, K.2    Yamamoto, H.3
  • 25
    • 34447500110 scopus 로고    scopus 로고
    • New boron(III)-catalyzed amide and ester condensation Reactions
    • Maki, T.; Ishihara, K.; Yamamoto, H. New boron(III)-catalyzed amide and ester condensation Reactions. Tetrahedron 2007, 63, 8645.
    • (2007) Tetrahedron , vol.63 , pp. 8645
    • Maki, T.1    Ishihara, K.2    Yamamoto, H.3
  • 26
    • 28944444304 scopus 로고    scopus 로고
    • Bulky diarylammonium arenesulfonates as mild and extremely active dehydrative ester condensation catalysts
    • Sakakura, A.; Nakagawa, S.; Ishihara, K. Bulky diarylammonium arenesulfonates as mild and extremely active dehydrative ester condensation catalysts. Tetrahedron 2006, 62, 422.
    • (2006) Tetrahedron , vol.62 , pp. 422
    • Sakakura, A.1    Nakagawa, S.2    Ishihara, K.3
  • 27
    • 16244400119 scopus 로고    scopus 로고
    • Bulky diarylammonium arenesulfonates as selective esterification catalysts
    • Ishihara, K.; Nakagawa, S.; Sakakura, A. Bulky diarylammonium arenesulfonates as selective esterification catalysts. J. Am. Chem. Soc. 2005, 127, 4168.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 4168
    • Ishihara, K.1    Nakagawa, S.2    Sakakura, A.3
  • 28
    • 34250794551 scopus 로고    scopus 로고
    • Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates
    • Sakakura, A.; Watanabe, H.; Nakagawa, S.; Ishihara, K. Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates. Chem. Asian J. 2007, 2, 477.
    • (2007) Chem. Asian J , vol.2 , pp. 477
    • Sakakura, A.1    Watanabe, H.2    Nakagawa, S.3    Ishihara, K.4
  • 29
    • 34548581078 scopus 로고    scopus 로고
    • Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates
    • Sakakura, A.; Nakagawa, S.; Ishihara, K. Direct ester condensation catalyzed by bulky diarylammonium pentafluorobenzenesulfonates. Nat. Protocols 2007, 2, 1746.
    • (2007) Nat. Protocols , vol.2 , pp. 1746
    • Sakakura, A.1    Nakagawa, S.2    Ishihara, K.3
  • 30
    • 36749050839 scopus 로고    scopus 로고
    • Widely useful DMAP-catalyzed esterification under auxiliary base-free and solvent-free conditions
    • Sakakura, A.; Kawajiri, K.; Ohkubo, T.; Kosugi, Y.; Ishihara, K. Widely useful DMAP-catalyzed esterification under auxiliary base-free and solvent-free conditions. J. Am. Chem. Soc. 2007, 129, 14775.
    • (2007) J. Am. Chem. Soc , vol.129 , pp. 14775
    • Sakakura, A.1    Kawajiri, K.2    Ohkubo, T.3    Kosugi, Y.4    Ishihara, K.5
  • 31
    • 46749125277 scopus 로고    scopus 로고
    • Open-air and solventfree ester condensation catalyzed by sulfonic acids
    • Sakakura, A.; Koshikari, Y.; Ishihara, K. Open-air and solventfree ester condensation catalyzed by sulfonic acids. Tetrahedron Lett. 2008, 49, 5017.
    • (2008) Tetrahedron Lett , vol.49 , pp. 5017
    • Sakakura, A.1    Koshikari, Y.2    Ishihara, K.3
  • 32
    • 0034234818 scopus 로고    scopus 로고
    • Diphenylammonium triflate (DPAT): Efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols
    • Wakasugi, K.; Misaki, T.; Yamada, K.; Tanabe, Y. Diphenylammonium triflate (DPAT): efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols. Tetrahedron Lett. 2000, 41, 5249.
    • (2000) Tetrahedron Lett , vol.41 , pp. 5249
    • Wakasugi, K.1    Misaki, T.2    Yamada, K.3    Tanabe, Y.4
  • 33
    • 33751359795 scopus 로고    scopus 로고
    • Pentafluorophenylammonium triflate (PFPAT): An efficient, practical, and costeffective catalyst for esterification, thioesterification, transesterification, and macrolactone formation
    • Funatomi, T.; Wakasugi, K.; Misaki, T.; Tanabe, Y. Pentafluorophenylammonium triflate (PFPAT): An efficient, practical, and costeffective catalyst for esterification, thioesterification, transesterification, and macrolactone formation. Green Chem. 2006, 8, 1022.
    • (2006) Green Chem , vol.8 , pp. 1022
    • Funatomi, T.1    Wakasugi, K.2    Misaki, T.3    Tanabe, Y.4
  • 35
    • 45449106974 scopus 로고    scopus 로고
    • 3(OTf) catalyzed efficient acylation of -OH and -SH: Direct esterification of alcohols with carboxylic acids and transesterification of alcohols with esters under neat conditions
    • 3(OTf) catalyzed efficient acylation of -OH and -SH: Direct esterification of alcohols with carboxylic acids and transesterification of alcohols with esters under neat conditions. J. Mol. Catal. A: Chem. 2008, 289, 61.
    • (2008) J. Mol. Catal. A: Chem , vol.289 , pp. 61
    • Firouzabadi, H.1    Iranpoor, N.2    Farahi, S.3
  • 36
    • 33847633832 scopus 로고    scopus 로고
    • Polymer-supported sulfonimide as a novel water-tolerant Brønsted acid catalyst for esterification of equimolar carboxylic acids and alcohols
    • Zhang, Z.; Zhou, S.; Nie, J. Polymer-supported sulfonimide as a novel water-tolerant Brønsted acid catalyst for esterification of equimolar carboxylic acids and alcohols. J. Mol. Catal. A: Chem. 2007, 265, 9.
    • (2007) J. Mol. Catal. A: Chem , vol.265 , pp. 9
    • Zhang, Z.1    Zhou, S.2    Nie, J.3
  • 37
    • 37349086512 scopus 로고    scopus 로고
    • A green approach for the synthesis of long chain aliphatic acid esters at room temperature
    • Li, X. W.; Eli, W. A green approach for the synthesis of long chain aliphatic acid esters at room temperature. J. Mol. Catal. A: Chem. 2008, 279, 159.
    • (2008) J. Mol. Catal. A: Chem , vol.279 , pp. 159
    • Li, X.W.1    Eli, W.2
  • 38
    • 23744470314 scopus 로고    scopus 로고
    • 2O catalyst. Synthesis 2005, 12, 1939.
    • 2O catalyst. Synthesis 2005, 12, 1939.
  • 39
    • 31544457398 scopus 로고    scopus 로고
    • Esterification of long chain aliphatic acids with long chain alcohols catalyzed by multivalent metal salts
    • Mantri, K.; Nakamura, R.; Komura, K.; Sugi, Y. Esterification of long chain aliphatic acids with long chain alcohols catalyzed by multivalent metal salts. Chem. Lett. 2005, 34, 1502.
    • (2005) Chem. Lett , vol.34 , pp. 1502
    • Mantri, K.1    Nakamura, R.2    Komura, K.3    Sugi, Y.4
  • 40
    • 24944541943 scopus 로고    scopus 로고
    • 2O catalysts for the esterification of long chain aliphatic carboxylic acids and alcohols. The enhancement of catalytic performance by supporting on ordered mesoporous silica. Green Chem. 2005, 7, 677.
    • 2O catalysts for the esterification of long chain aliphatic carboxylic acids and alcohols. The enhancement of catalytic performance by supporting on ordered mesoporous silica. Green Chem. 2005, 7, 677.
  • 41
    • 36549072397 scopus 로고    scopus 로고
    • The esterification of glycerine with lauric acid catalyzed by multi-valent metal salts. Selective formation of mono- and dilaurins
    • Nakamura, R.; Komura, K.; Sugi, Y. The esterification of glycerine with lauric acid catalyzed by multi-valent metal salts. Selective formation of mono- and dilaurins. Catal. Commun. 2007, 9, 2302.
    • (2007) Catal. Commun , vol.9 , pp. 2302
    • Nakamura, R.1    Komura, K.2    Sugi, Y.3
  • 42
    • 56249087188 scopus 로고    scopus 로고
    • 2O as a Versatile Catalyst for the Esterification of Steroid Alcohols with Fatty Acids. Synthesis 2008, in press.
    • 2O as a Versatile Catalyst for the Esterification of Steroid Alcohols with Fatty Acids. Synthesis 2008, in press.
  • 44
    • 0001304091 scopus 로고
    • The crystal structure of zirconyl chloride octahydrate and zirconyl bromide octahydrate
    • Clearfield, A.; Vaughan, P. A. The crystal structure of zirconyl chloride octahydrate and zirconyl bromide octahydrate. Acta Crystallogr. 1956, 9, 555.
    • (1956) Acta Crystallogr , vol.9 , pp. 555
    • Clearfield, A.1    Vaughan, P.A.2


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