Highly selective synthesis of menthols from citral in a one-step process

被引:76
|
作者
Trasarti, AF [1 ]
Marchi, AJ [1 ]
Apesteguia, CR [1 ]
机构
[1] UNL, CONICET, Catalysis Sci & Engn Res Grp, Inst Invest Catalisis & Petroquim, RA-3000 Santa Fe, Argentina
关键词
menthol synthesis; citral conversion; fine chemistry; sustainable processes;
D O I
10.1016/j.jcat.2004.03.016
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
We report for the first time the selective synthesis of menthols from citral in a one-step process. Bifunctional metal/acid catalysts active and selective for menthol synthesis were developed by studying the individual steps involved in the reaction pathway leading to menthols from citral. The metallic component was selected by testing silica-supported metals for citral hydrogenation to citronellal. Acid site requirements to efficiently isomerize citronellal to isopulegols were investigated on different solid acids. Potential bifunctional metal/acid catalysts were then prepared and tested for citral conversion to menthols. The best catalyst was Ni/Al-MCM-41, which yielded about 90% menthols and cave 70-75% of racemic (+/-)-menthol in the menthol mixture. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:484 / 488
页数:5
相关论文
共 50 条
  • [41] ONE-STEP SYNTHESIS OF (+/-)-FRONTALIN
    KONGKATHIP, N
    KONGKATHIP, B
    JOURNAL OF THE SCIENCE SOCIETY OF THAILAND, 1992, 18 (04): : 225 - 227
  • [42] One-step synthesis of isocorroles
    Nardis, Sara
    Pomarico, Giuseppe
    Fronczek, Frank R.
    Vicente, Maria Graca H.
    Paolesse, Roberto
    TETRAHEDRON LETTERS, 2007, 48 (49) : 8643 - 8646
  • [43] One-Step Synthesis of Normoftal
    A. N. Balaev
    E. V. Reshetnikov
    V. E. Fedorov
    Pharmaceutical Chemistry Journal, 2014, 48 : 49 - 50
  • [44] One-Step Synthesis of Normoftal
    Balaev, A. N.
    Reshetnikov, E. V.
    Fedorov, V. E.
    PHARMACEUTICAL CHEMISTRY JOURNAL, 2014, 48 (01) : 49 - 50
  • [45] One-step synthesis of diphenyhnethanes
    Wei, QY
    Luo, YG
    Zhou, M
    Tao, FY
    Zhang, GL
    SYNTHETIC COMMUNICATIONS, 2005, 35 (06) : 835 - 843
  • [46] A ONE-STEP SYNTHESIS OF DIHYDROFLAVONOLS
    MULCHANDANI, NB
    CHADHA, MS
    CHEMISTRY & INDUSTRY, 1964, (36) : 1554 - 1554
  • [47] ONE-STEP SYNTHESIS OF DODECAMETHYLCYCLOHEXASILANE
    LAGUERRE, M
    DUNOGUES, J
    CALAS, R
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1978, (06) : 272 - 272
  • [48] ONE-STEP SYNTHESIS OF CYCLOPENTADIENYLCHLOROSILANES
    KOSHUTIN, VI
    MAKSIMOVA, LN
    EMYASHEV, VI
    SMIRNOV, VA
    ZHURNAL OBSHCHEI KHIMII, 1976, 46 (01): : 146 - 150
  • [49] EIGENVALUES FOR A ONE-STEP PROCESS IN ONE DIMENSION
    MALASPINAS, A
    JOURNAL OF PHYSICS A-MATHEMATICAL AND GENERAL, 1986, 19 (04): : 547 - 550
  • [50] Lewis pair catalyzed highly selective polymerization for the one-step synthesis of AzCy(AB)xCyAz pentablock terpolymers
    Zhu, Shuaishuai
    Wang, Yong
    Ding, Wanzhi
    Zhou, Xingping
    Liao, Yonggui
    Xie, Xiaolin
    POLYMER CHEMISTRY, 2020, 11 (10) : 1691 - 1695