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Linalool Synthesis from α-Pinene: Kinetic Peculiarities of Catalytic Steps Full article

Journal Applied Catalysis A: General
ISSN: 0926-860X , E-ISSN: 1873-3875
Output data Year: 2001, Volume: 211, Number: 1, Pages: 91-107 Pages count : 17 DOI: 10.1016/S0926-860X(00)00841-3
Tags Aromatic compounds; Catalyst selectivity; Hydrogenation; Isomerization; Oxidation; Reaction kinetics; Synthesis (chemical)
Authors Semikolenov V.A. 1 , Ilʹina I.I. 1 , Simakova I.L. 1
Affiliations
1 Boreskov Institute of Catalysis, Prospekt Akademika Lavrentieva 5, Novosibirsk, 630090, Russia

Abstract: Synthesis of linalool from α-pinene which includes consecutively α-pinene hydrogenation to pinane on Pd/C catalyst, pinane oxidation to pinane-hydroperoxide by molecular oxygen and pinane-hydroperoxide hydrogenation to pinanol on Pd/C catalyst followed by its thermal isomerization to linalool is discussed. The effects of the reagent concentrations, temperature and catalyst content on the reaction rate and selectivity are studied. The kinetic peculiarities and the mechanisms of reactions are presented. The synthetic conditions of high-selective linalool preparation are found.
Cite: Semikolenov V.A. , Ilʹina I.I. , Simakova I.L.
Linalool Synthesis from α-Pinene: Kinetic Peculiarities of Catalytic Steps
Applied Catalysis A: General. 2001. V.211. N1. P.91-107. DOI: 10.1016/S0926-860X(00)00841-3 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Mar 21, 2000
Accepted: Oct 31, 2000
Published online: Mar 7, 2001
Published print: Mar 16, 2001
Identifiers:
Web of science: WOS:000167626600009
Scopus: 2-s2.0-0035278461
Elibrary: 13374066
Chemical Abstracts: 2001:177560
Chemical Abstracts (print): 135:5711
OpenAlex: W2061399244
Citing:
DB Citing
Web of science 55
Scopus 65
Elibrary 62
OpenAlex 56
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