Solid Lewis Acids Catalyze the Carbon-Carbon Coupling between Carbohydrates and Formaldehyde

被引:106
作者
Van de Vyver, Stijn [1 ]
Odermatt, Caroline [1 ]
Romero, Kevin [1 ]
Prasomsri, Teerawit [1 ]
Roman-Leshkov, Yuriy [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
来源
ACS CATALYSIS | 2015年 / 5卷 / 02期
关键词
aldol condensation; biomass conversion; heterogeneous catalysis; isotope labeling studies; proton transfer; Sn-Beta; soft enolization; solid Lewis acid; SN-BETA ZEOLITE; BAEYER-VILLIGER OXIDATIONS; PONNDORF-VERLEY REDUCTION; GAMMA-VALEROLACTONE; CYCLIC-KETONES; BOND FORMATION; CONVERSION; WATER; ISOMERIZATION; MECHANISM;
D O I
10.1021/cs5015964
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 development of catalytic C-C bond formation schemes based on renewable substrates is important for defining sustainable paradigms for chemical manufacturing. With a few exceptions, aldol condensation reactions between biomass-derived platform chemicals have received little attention so far. Here the C-C coupling between 1,3-dihydroxyacetone (DHA) and formaldehyde into alpha-hydroxy-gamma-butyrolactone (HBL) using Sn-Beta is demonstrated. Reactivity studies, coupled with spectroscopic and computational analyses, show that the formation of HBL proceeds by soft enolization of DHA followed by an aldol addition of formaldehyde to the Sn-enolate intermediate, generating erythrulose as an intermediate species. Isotopic labeling is used to reveal the position where formaldehyde is incorporated into HBL, providing further support for our proposed mechanism. Finally, combining the C-C coupling reaction with transfer hydrogenation of formaldehyde has allowed us to expand the substrate scope to include polyols glycerol and ethylene glycol.
引用
收藏
页码:972 / 977
页数:6
相关论文
共 52 条
  • [1] Nopol production over Sn-MCM-41 synthesized by different procedures - Solvent effects
    Alarcon, Edwin A.
    Correa, Luis
    Montes, Consuelo
    Luz Villa, Aida
    [J]. MICROPOROUS AND MESOPOROUS MATERIALS, 2010, 136 (1-3) : 59 - 67
  • [2] Characterization of two lactones in liquid phase: an experimental and computational approach
    Aparicio, Santiago
    Alcalde, Rafael
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (30) : 6455 - 6467
  • [3] Exploring Meerwein-Ponndorf-Verley Reduction Chemistry for Biomass Catalysis Using a First-Principles Approach
    Assary, Rajeev S.
    Curtiss, Larry A.
    Dumesic, James A.
    [J]. ACS CATALYSIS, 2013, 3 (12): : 2694 - 2704
  • [4] Theoretical study of the mutarotation of erythrose and threose: acid catalysis
    Azofra, Luis Miguel
    Alkorta, Ibon
    Elguero, Jose
    [J]. CARBOHYDRATE RESEARCH, 2013, 372 : 1 - 8
  • [5] Metalloenzyme-like catalyzed isomerizations of sugars by Lewis acid zeolites
    Bermejo-Deval, Ricardo
    Assary, Rajeev S.
    Nikolla, Eranda
    Moliner, Manuel
    Roman-Leshkov, Yuriy
    Hwang, Son-Jong
    Palsdottir, Arna
    Silverman, Dorothy
    Lobo, Raul F.
    Curtiss, Larry A.
    Davis, Mark E.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (25) : 9727 - 9732
  • [6] Domino Reaction Catalyzed by Zeolites with BrOnsted and Lewis Acid Sites for the Production of -Valerolactone from Furfural
    Bui, Linh
    Luo, Helen
    Gunther, William R.
    Roman-Leshkov, Yuriy
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (31) : 8022 - 8025
  • [7] Centi G., 2007, CATALYSIS RENEWABLES, P27
  • [8] Acetalization of ethylene glycol with formaldehyde using cation-exchange resins as catalysts: batch versus reactive distillation
    Chopade, SP
    Sharma, MM
    [J]. REACTIVE & FUNCTIONAL POLYMERS, 1997, 34 (01) : 37 - 45
  • [9] Clayden J., 2012, ORGANIC CHEM, P256
  • [10] Sn-Beta zeolite as diastereoselective water-resistant heterogeneous Lewis-acid catalyst for carbon-carbon bond formation in the intramolecular carbonyl-ene reaction
    Corma, A
    Renz, M
    [J]. CHEMICAL COMMUNICATIONS, 2004, (05) : 550 - 551