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Volumn 85, Issue 12, 2010, Pages 1663-1670

Solvent-free synthesis of glycerol carbonate and glycidol from 3-chloro-1,2-propanediol and potassium (hydrogen) carbonate

Author keywords

3 chloro 1,2 propanediol; Glycerol; Glycerol carbonate; Glycidol; Potassium (hydrogen)carbonate

Indexed keywords

DIRECT REACTIONS; EXPERIMENTAL CONDITIONS; GLYCEROL CARBONATE; GLYCIDOL; HIGH YIELD; MOLAR RATIO; OPERATING CONDITION; PROPANEDIOLS; REACTION TIME; SOLVENT FREE; SOLVENT FREE SYNTHESIS; SYNTHETIC APPROACH; SYNTHETIC STRATEGIES;

EID: 78349250152     PISSN: 02682575     EISSN: 10974660     Source Type: Journal    
DOI: 10.1002/jctb.2478     Document Type: Article
Times cited : (26)

References (26)
  • 1
    • 78349293120 scopus 로고    scopus 로고
    • The Future of Glycerol, New Usages for a Versatile Raw Material
    • Pagliaro M and Rossi M (eds), RSC Green Chemistry Book Series. RSC Publishing, Cambridge
    • Pagliaro M and Rossi M (eds), Sustainability of bioglycerol in The Future of Glycerol, New Usages for a Versatile Raw Material. RSC Green Chemistry Book Series. RSC Publishing, Cambridge,109-123 (2008).
    • (2008) Sustainability of bioglycerol , pp. 109-123
  • 2
    • 77954384216 scopus 로고    scopus 로고
    • (eds), Top value added chemicals from biomass, Results of screening for potential candidates from sugars and synthesis gas. The Pacific Northwest Laboratory and The National Renewable Energy Laboratory, U.S. Department of Energy, Office of Scientific and Technical Information, N°. DOE/GO-102004-1992 (accessed, February 20, 2010).
    • Werpy T and Petersen G (eds), Top value added chemicals from biomass, Vol. I-Results of screening for potential candidates from sugars and synthesis gas. The Pacific Northwest Laboratory and The National Renewable Energy Laboratory, U.S. Department of Energy, Office of Scientific and Technical Information, N°. DOE/GO-102004-1992 (2004). (accessed, February 20, 2010).
    • (2004) , vol.1
    • Werpy, T.1    Petersen, G.2
  • 3
    • 0037023397 scopus 로고    scopus 로고
    • Nucleophilic catalysis with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) for the esterification of carboxylic acids with dimethyl carbonate
    • Shieh W-C, Dell S and Repič O, Nucleophilic catalysis with 1, 8-diazabicyclo[5.4.0]undec-7-ene (DBU) for the esterification of carboxylic acids with dimethyl carbonate. J Org Chem 67: 2188-2191 (2002).
    • (2002) J Org Chem , vol.67 , pp. 2188-2191
    • Shieh, W.1    Dell, S.2    Repič, O.3
  • 4
    • 37849012760 scopus 로고    scopus 로고
    • Improved utilisation of renewable resources: new important derivatives of glycerol
    • Bher A, Eilting J, Irawadi K, Leschinski J and Lindner F, Improved utilisation of renewable resources: new important derivatives of glycerol. Green Chem 10: 13-30 (2008).
    • (2008) Green Chem , vol.10 , pp. 13-30
    • Bher, A.1    Eilting, J.2    Irawadi, K.3    Leschinski, J.4    Lindner, F.5
  • 5
    • 78349298770 scopus 로고    scopus 로고
    • Method for producing an epoxyde, in particular of glycidol, and installation for implementation. World Intellectual Property Organization Pat. WO 9840371
    • Yoo J-W, Mouloungui Z and Gaset A, Method for producing an epoxyde, in particular of glycidol, and installation for implementation. World Intellectual Property Organization Pat. WO 9840371 (1998).
    • (1998)
    • Yoo, J.1    Mouloungui, Z.2    Gaset, A.3
  • 6
    • 0036569283 scopus 로고    scopus 로고
    • Carbon dioxide separation with novel solvents as liquid membranes
    • Kovvali AS and Sirkar KK, Carbon dioxide separation with novel solvents as liquid membranes. Ind Eng Chem Res 41: 2287-2295 (2002).
    • (2002) Ind Eng Chem Res , vol.41 , pp. 2287-2295
    • Kovvali, A.S.1    Sirkar, K.K.2
  • 7
    • 78349256745 scopus 로고    scopus 로고
    • The Future of Glycerol, New Usages for a Versatile Raw Material
    • Pagliaro M and Rossi M (eds), RSC Green Chemistry Book Series. RSC Publishing, Cambridge
    • Pagliaro M and Rossi M (eds), Esterification, in The Future of Glycerol, New Usages for a Versatile Raw Material. RSC Green Chemistry Book Series. RSC Publishing, Cambridge,73-85 (2008).
    • (2008) Esterification , pp. 73-85
  • 8
    • 78349266562 scopus 로고    scopus 로고
    • Process for the preparation of glycerol carbonate from glycerol and a cyclic organic carbonate, especially ethylene or propylene carbonate. European Patent 0739888
    • Mouloungui Z, Yoo J-W, Gachen C-A, Gaset A and Vermeersch G, Process for the preparation of glycerol carbonate from glycerol and a cyclic organic carbonate, especially ethylene or propylene carbonate. European Patent 0739888 (1996).
    • (1996)
    • Mouloungui, Z.1    Yoo, J.2    Gachen, C.3    Gaset, A.4    Vermeersch, G.5
  • 9
    • 35448955322 scopus 로고    scopus 로고
    • Lipase-catalyzed synthesis of glycerol carbonate from renewable glycerol and dimethyl carbonate through transesterification
    • Kim SC, Kim YH, Lee H, Yoon DY and Song BK, Lipase-catalyzed synthesis of glycerol carbonate from renewable glycerol and dimethyl carbonate through transesterification. J Mol Catal B: Enzym 49: 75-78 (2007).
    • (2007) J Mol Catal B: Enzym , vol.49 , pp. 75-78
    • Kim, S.C.1    Kim, Y.H.2    Lee, H.3    Yoon, D.Y.4    Song, B.K.5
  • 11
    • 22544459626 scopus 로고    scopus 로고
    • Hyperbranched aliphatic polyethers obtained from environmentally benign monomer: glycerol carbonate
    • Rokicki G, Rakoczy P, Parzuchowski P and Sobiecki M, Hyperbranched aliphatic polyethers obtained from environmentally benign monomer: glycerol carbonate. Green Chem 7: 529-539 (2005).
    • (2005) Green Chem , vol.7 , pp. 529-539
    • Rokicki, G.1    Rakoczy, P.2    Parzuchowski, P.3    Sobiecki, M.4
  • 12
    • 68949130175 scopus 로고    scopus 로고
    • Imidazolium-2-carboxylate as an efficient, expeditious and eco-friendly organocatalyst for glycerol carbonate synthesis
    • Naik PU, Petitjean L, Refes K, Picquet M and Plasseraud L, Imidazolium-2-carboxylate as an efficient, expeditious and eco-friendly organocatalyst for glycerol carbonate synthesis. Adv Synth Catal 351: 1753-1756 (2009).
    • (2009) Adv Synth Catal , vol.351 , pp. 1753-1756
    • Naik, P.U.1    Petitjean, L.2    Refes, K.3    Picquet, M.4    Plasseraud, L.5
  • 13
    • 78349253523 scopus 로고
    • Preparation of glyceryl carbonate. US Patent 5359094
    • Teles JH, Rieber N and Harder W, Preparation of glyceryl carbonate. US Patent 5359094 (1994).
    • (1994)
    • Teles, J.H.1    Rieber, N.2    Harder, W.3
  • 14
    • 78349248710 scopus 로고    scopus 로고
    • Method for preparing glycerol carbonate. US Patent 6025504
    • Claude S, Mouloungui Z, Yoo J-W and Gaset A, Method for preparing glycerol carbonate. US Patent 6025504 (1999).
    • (1999)
    • Claude, S.1    Mouloungui, Z.2    Yoo, J.3    Gaset, A.4
  • 15
    • 78349235503 scopus 로고    scopus 로고
    • Process for the preparation of glycerol carbonate. US Patent 6495703
    • Okutsu M and Kitsuki T, Process for the preparation of glycerol carbonate. US Patent 6495703 (2002).
    • (2002)
    • Okutsu, M.1    Kitsuki, T.2
  • 16
    • 0001145537 scopus 로고
    • Epoxidation of allyl alcohol to glycidol using titanium silicalite TS-1: effect of the method of preparation
    • Hutchings GJ, Lee DF and Minihan AR, Epoxidation of allyl alcohol to glycidol using titanium silicalite TS-1: effect of the method of preparation. Catal Lett 33: 369-385 (1995).
    • (1995) Catal Lett , vol.33 , pp. 369-385
    • Hutchings, G.J.1    Lee, D.F.2    Minihan, A.R.3
  • 17
    • 0000761844 scopus 로고
    • Kirk-Othmer Encyclopedia of Chemical Technology
    • 4th edn, ed by Kroschwitz JI and Howe-Grant M. John Wiley, New York
    • Richey WF, Chlorohydrins, in Kirk-Othmer Encyclopedia of Chemical Technology, 4th edn, ed by Kroschwitz JI and Howe-Grant M. John Wiley, New York, Vol. 6,140-155 (1993).
    • (1993) Chlorohydrins , vol.6 , pp. 140-155
    • Richey, W.F.1
  • 18
    • 78349279673 scopus 로고    scopus 로고
    • Process for production of glycidol. European patent 2028181 A1
    • Uno M and Okutsu M, Process for production of glycidol. European patent 2028181 A1 (2009).
    • (2009)
    • Uno, M.1    Okutsu, M.2
  • 19
    • 78349303129 scopus 로고    scopus 로고
    • Process for manufacturing glycidol. World Intellectual Property Organization Pat. WO 2009/016149 A2
    • Gilbeau P. Process for manufacturing glycidol. World Intellectual Property Organization Pat. WO 2009/016149 A2 (2009).
    • (2009)
    • Gilbeau, P.1
  • 21
    • 33748289995 scopus 로고    scopus 로고
    • A study on the carboxylation of glycerol to glycerol carbonate with carbon dioxide: the role of the catalyst, solvent and reaction conditions
    • Aresta M, Dibenedetto A, Nocito F and Pastore C, A study on the carboxylation of glycerol to glycerol carbonate with carbon dioxide: the role of the catalyst, solvent and reaction conditions. J Mol Catal A: Chem 257: 149-153 (2006).
    • (2006) J Mol Catal A: Chem , vol.257 , pp. 149-153
    • Aresta, M.1    Dibenedetto, A.2    Nocito, F.3    Pastore, C.4
  • 24
    • 0020289711 scopus 로고
    • A new route to carbonate monomers for synthesis of polycarbonates
    • Rokicki G, Pawlicki J and Kuran W, A new route to carbonate monomers for synthesis of polycarbonates. Polym J 14: 839-845 (1982).
    • (1982) Polym J , vol.14 , pp. 839-845
    • Rokicki, G.1    Pawlicki, J.2    Kuran, W.3
  • 25
    • 75449086645 scopus 로고    scopus 로고
    • A quantitative structure property relation correlation of the dielectric constant for organic chemicals
    • Liu JP, Wilding WV, Giles NF and Rowley RL, A quantitative structure property relation correlation of the dielectric constant for organic chemicals. J Chem Eng Data 55: 41-45 (2010).
    • (2010) J Chem Eng Data , vol.55 , pp. 41-45
    • Liu, J.P.1    Wilding, W.V.2    Giles, N.F.3    Rowley, R.L.4
  • 26
    • 0013362285 scopus 로고
    • Room temperature polymerization of glycidol
    • Sandler SR and Berg FR, Room temperature polymerization of glycidol. J Polym Sci A: Polym Chem 4: 1253-1259 (1966).
    • (1966) J Polym Sci A: Polym Chem , vol.4 , pp. 1253-1259
    • Sandler, S.R.1    Berg, F.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.