The Formation Mechanism of Trimethylpentanes from Esters in Liquid Phase Alkylation of Isobutane with Butenes
- Authors: Katsman Е.А.1
-
Affiliations:
- MIREA – Russian Technological University
- Issue: Vol 65, No 4 (2024)
- Pages: 485-492
- Section: ARTICLES
- URL: https://rjeid.com/0453-8811/article/view/684234
- DOI: https://doi.org/10.31857/S0453881124040098
- EDN: https://elibrary.ru/RHLKDQ
- ID: 684234
Cite item
Abstract
The formation sequence of trimethylpentane (TMP) isomers during liquid phase interaction of butyltriflates and butenes with isobutene studied. In the alkylation products composition isomers of TMP share during homogeneous interaction in isobutane forms a row 2,2,4 > 2,3,4 > 2,3,3 >> 2,2,3, but in two-phase system isobutene–tryflic acid – 2,3,4 > 2,3,3 > 2,2,4 >> 2,2,3. As reaction time elongates the isomer composition approximate to composition of usual marketable product mainly owing to isomerization of 2,3,4- and 2,3,3-isomers into 2,2,4-isomer. The peculiarities of possible formation mechanisms of primary reaction products discussed. They are in the case of butenes 2,2,4- и 2,2,3-TMP, and in the case of butyltriflates – 2,3,4- и 2,3,3-TMP.
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About the authors
Е. А. Katsman
MIREA – Russian Technological University
Author for correspondence.
Email: katsman@aha.ru
Russian Federation, Moscow
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