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DOI: 10.1055/s-0030-1260825
Lithium Dibenzylamide, a Simple, Selective and Highly Efficient Catalyst for Isocyanate Cyclotrimerization to Isocyanurate
Publication History
Publication Date:
28 June 2011 (online)

Abstract
Lithium dibenzylamide catalyzed the rapid and essentially quantitative cyclotrimerization of a variety of isocyanates under mild conditions and could be recycled for six times in high yield.
Key words
lithium amides - catalysis - isocyanates cyclotrimerization - isocyanurates
- Supporting Information for this article is available online:
- Supporting Information
- Primary data for this article are available online and can be cited using the following DOI: 10.4125/pd0013th:
- Primary Data
- 1
Kordomenos PI.Kresta JE.Frisch KC. ACS. Org. Coat. Plast. Chem. Preprints 1978, 38: 450 - 2
Duong HA.Cross MJ.Louie J. Org. Lett. 2004, 6: 4679 - 3
Wirpsza Z. Polyurethanes: Chemistry, Technology and Application Ellis Horwood; London: 1993. - 4
Zitinkina AK.Sibanova NA.Tarakanov OG. Russ. Chem. Rev. (Engl. Transl.) 1985, 54: 1104 - 5
Nawata T.Kresta JE.Frisch KC. J. Cell. Plast. 1975, 267 - 6
Nicholas L.Gmitter GR. J. Cell. Plast. 1965, 85 - 7
Tang J.Mohan T.Verkade JG. J. Org. Chem. 1994, 59: 4931 - 8
Raders SM.Verkade JG. J. Org. Chem. 2010, 75: 5308 - 9
Sugimoto H.Yamane Y.Inoue S. Tetrahedron: Asymmetry 2000, 11: 2067 - 10
Murray AP.Miller MJ. J. Org. Chem. 2003, 68: 191 - 11
Bukac Z.Sebenda J. Chem. Prum. 1985, 35: 361 - 12
Horsky J.Kubanek U.Marick J.Kralicek J. Chem. Prum. 1982, 32: 599 - 13
Liu X.Bai Y.Verkade JG. J. Organomet. Chem. 1999, 582: 16 - 14
Orzechowski L.Harder S. Organometallics 2007, 26: 2144 - 15
Pawar GM.Buchmeiser MR. Adv. Synth. Catal. 2010, 352: 917 - 16
Kogon IC. J. Am. Chem. Soc. 1956, 78: 4911 - 17
Moghaddam FM.Dekamin MG.Koozehgari GR. Lett. Org. Chem. 2005, 2: 734 - 18
Villa JF.Powell HB. Synth. React. Inorg. Metal-Org. Chem. 1976, 6: 59 - 19
Nambu Y.Endo T. J. Org. Chem. 1993, 58: 1932 - 20
Mizura J.Yokozawa T.Endo T. J. Polym. Sci. Polym. Chem. Ed. 1991, 29: 1545 - 21
Moghaddam FM.Dekamin MG.Khajavi MS.Jalili S. Bull. Chem. Soc. Jpn. 2002, 75: 851 - 22
Tanimoto F.Tanka T.Kitano H.Fukui K. Bull. Chem. Soc. Jpn. 1996, 39: 1922 - 23
Khajavi MS.Dakamin MG.Hazarkhani H. J. Chem. Res., Synop. 2000, 145 - 24
Foley SR.Yap GPA.Richeson DS. Organometallics 1999, 18: 4700 - 25
Li Y.Matsumura H.Yamanaka M.Takahashi T. Tetrahedron 2004, 60: 1393 - 26
Noltes JG.Boersma J. J. Organomet. Chem. 1967, 7: P6 - 27
Wu YJ.Wang SW.Zhu XC. Inorg. Chem. 2008, 47: 5503 - 28
Zhu XC.Fan JX.Wu YJ. Organometallics 2009, 28: 3882 - 29
Paul F.Moulin S.Piechaczyk O.Le Floch P.Osborn JA. J. Am. Chem. Soc. 2007, 129: 7294
References and Notes
Representative Procedure: An oven-dried Schlenk tube under nitrogen was charged with phenyl isocyanate, lithium dibenzylamide (0.1 mol%), and Et2O (30 mL). The reaction mixture was stirred at r.t. for 2 min. The resulting precipitate was filtered off, washed with Et2O (3 × 3 mL), and dried under reduced pressure to give the isocyanurate 1,3,5-triphenyl-1,3,5-triazinane-2,4,6-trione (1) as a white solid.
31Procedure for Recycling Experiment of Lithium Dibenzylamide: Phenyl isocyanate was added to a solution of lithium dibenzylamide (0.1 mol%) in Et2O (30 mL) with stirring. The reaction mixture was stirred at r.t. for the allotted time and filtered via a canula filter. The Et2O filtrate was subjected to a second reaction cycle. This procedure was repeated six times (for details see Table [³] ).