Efficient synthesis of 1,4-diazabicyclo(2.2.2) octane in ionic liquids

被引:2
|
作者
Zhao, Dishun [1 ,2 ]
Duan, Erhong [1 ]
Liu, Ran [2 ]
Xiao, Qianru [2 ]
Fan, Shiming [2 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Hebei Univ Sci & Technol, Sch Chem & Pharmaceut Engn, Shijiazhuang 050018, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
synthesis; 1,4-diazabicyclo(2.2.2)octane; ionic liquid; catalysis;
D O I
10.1016/j.catcom.2008.01.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The synthesis process of 1,4-diazabicyclo(2.2.2) octane by reaction of ethylenediamine or monoethanolamine, for the first time, was achieved in the presence of ionic liquids. The comparative study showed that [Bmim][BF4] was more suitable to prepare 1,4-diazabicyclo(2.2.2)octane, with relatively high yield (up to 68.0%) and selectivity (ca. 72.6%). The reuse of [Bmim][BF4] was also studied. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1725 / 1727
页数:3
相关论文
共 50 条
  • [21] CRYSTALLINE COMPLEX OF CARBON TETRABROMIDE AND 1,4-DIAZABICYCLO[2.2.2]OCTANE
    LORAND, JP
    TETRAHEDRON LETTERS, 1971, (27) : 2511 - &
  • [22] Polymorphism of 1,4-diazabicyclo[2.2.2]octane complexes with HI and HBr
    Olejniczak, Anna
    Nowicki, Waldemar
    Katrusiak, Andrzej
    ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2011, 67 : C504 - C504
  • [23] 1,4-Diazabicyclo[2.2.2]octane (DABCO) 5-aminotetrazolates
    Laus, Gerhard
    Kahlenberg, Volker
    Wurst, Klaus
    Hummel, Michael
    Schottenberger, Herwig
    CRYSTALS, 2012, 2 (01): : 96 - 104
  • [24] DIAMMONIUM SALTS DERIVED FROM 1,4-DIAZABICYCLO[2.2.2]OCTANE
    BAYADA, A
    LAWRANCE, GA
    MAEDER, M
    AUSTRALIAN JOURNAL OF CHEMISTRY, 1994, 47 (01) : 7 - 13
  • [25] Third-generation ionic liquids with N-alkylated 1,4-diazabicyclo[2.2.2]octane cations and pelargonate anions
    Turgula, Anna
    Stesik, Konrad
    Materna, Katarzyna
    Klejdysz, Tomasz
    Praczyk, Tadeusz
    Pernak, Juliusz
    RSC ADVANCES, 2020, 10 (15) : 8653 - 8663
  • [26] KINETICS OF FORMATION OF URETHANES CATALYZED BY 1,4-DIAZABICYCLO[2.2.2]OCTANE
    TITSKII, GD
    GARKUSHABOZHKO, IP
    SAVELOVA, VA
    ZHURNAL ORGANICHESKOI KHIMII, 1989, 25 (05): : 938 - 941
  • [27] DEALKYLATION OF QUATERNARY AMMONIUM SALTS WITH 1,4-DIAZABICYCLO[2.2.2]OCTANE
    HO, TL
    SYNTHESIS-STUTTGART, 1972, (12): : 702 - 702
  • [28] catena-Poly[[aquadicinnamatocadmium]-μ-1,4-diazabicyclo[2.2.2]octane]
    Qu, Y
    Liu, ZD
    Tan, MY
    Zhu, HL
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2005, 61 : M420 - M422
  • [29] Efficient Baylis-Hillman Reaction via a 1,4-Diazabicyclo[2.2.2]octane-based Ionic Catalyst
    Yueqin Cai
    Ye Liu
    Guohua Gao
    Monatshefte für Chemie - Chemical Monthly, 2007, 138 : 1163 - 1166
  • [30] Efficient Baylis-Hillman reaction via a 1,4-diazabicyclo[2.2.2]octane-based ionic catalyst
    Cai, Yueqin
    Liu, Ye
    Gao, Guohua
    MONATSHEFTE FUR CHEMIE, 2007, 138 (11): : 1163 - 1166