Heteropoly acid catalysts in upgrading of biorenewables: Cycloaddition of aldehydes to monoterpenes in green solvents

被引:27
|
作者
Cotta, Rafaela F. [1 ]
da Silva Rocha, Kelly A. [2 ]
Kozhevnikova, Elena F. [3 ]
Kozhevnikov, Ivan V. [3 ]
Gusevskaya, Elena V. [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Quim, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Ouro Preto, Dept Quim, BR-35400000 Ouro Preto, MG, Brazil
[3] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
基金
英国工程与自然科学研究理事会;
关键词
Biomass-based feedstock; Cycloaddition; Green solvents; Heterogeneous acid catalysis; Monoterpenes; ALPHA-PINENE OXIDE; FRAGRANCE COMPOUNDS; ISOMERIZATION; CHEMISTRY; HYDRATION; TERPENES; ACETOXYLATION; VALORIZATION; CONVERSION; CAMPHENE;
D O I
10.1016/j.apcatb.2017.05.055
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
Acidic Cs salt of tungstophosphoric heteropoly acid, Cs2.5H0.5PW12O40 (CsPW), is excellent solid acid catalyst for liquid-phase cycloaddition reactions of biomass-based and easily available from essential oils monoterpenic compounds, such as limonene, alpha-terpineol, alpha-pinene, beta-pinene and nerol, with aldehydes, including benzaldehyde, crotonaldehyde as well as biomass-derived cuminaldehyde and trans-cinnamaldehyde. The reactions give oxabicyclo[3.3.1]nonene compounds potentially useful for the fragrance and pharmaceutical industries in good to excellent yields. The process is environmentally benign and can be performed in biomass-derived solvent 2-methyltetrahydrofuran and eco-friendly "green" organic solvents such as dimethylcarbonate and diethylcarbonate under mild conditions at low catalyst loadings without leaching problems. The solid CsPW catalyst can be easily separated from the reaction media and low-boiling solvents can be removed by distillation. Silica-supported H3PW12O40 also demonstrated good performance in these reactions. (C) 2017 Elsevier B.V. All rights reserved.
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页码:92 / 99
页数:8
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