Trifluoroacetic acid promoted hydration of styrene catalyzed by sulfonic resins: Comparison of the reactivity of styrene, n-hexene and cyclohexene

被引：15

作者：

Bianchini, Edoardo ^{[1
]}

Pietrobon, Luca ^{[1
]}

Ronchin, Lucio ^{[1
]}

Tortato, Claudio ^{[1
]}

Vavasori, Andrea ^{[1
]}

机构：

[1] Univ Ca Foscari Venice, Dept Mol Sci & Nanosyst, Campus Sci,Via Torino 155, I-30170 Venice, Italy

来源：

APPLIED CATALYSIS A-GENERAL | 2019年 / 570卷

关键词：

Trifluoroacetic acid; Acid catalysis; Olefin; Hydration; Cyclohexanol; ION-EXCHANGE-RESINS; ONE-POT SYNTHESIS; BECKMANN REARRANGEMENT; DISTILLATION PROCESS; RUTHENIUM CATALYSTS; FORMIC-ACID; HYDROGENATION; BENZENE; EQUILIBRIUM; COMPOSITES;

D O I：

10.1016/j.apcata.2018.11.014

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：

Alcohol production by olefin hydration is an important reaction in the modem intermediate chemistry. The use of trifluoroacetic acid (TFA) could be a way to increase alcohol productivity by addition of the TFA to the double bond forming the corresponding ester. The product obtained by addition is then hydrolyzed to alcohol by sulfonic resins. The study of the overall multiphase equilibrium aqueous TFA solution/olefin ester cyclohexene is carried out together with the initial rate of reaction for cyclohexene hydration. Reaction profiles and a likely reaction path is also given. The influence of the operative variable on both equilibria and initial reaction rate are studied in the range of temperature typical of the sulfonic resin as catalysts (383-413 K). The use of aqueous TFA allows fast reaction and high conversion as well as an easily separable aqueous system compared with other organic acid.

引用

页码：130 / 138

页数：9

共 54 条

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