Back to Search Start Over

Competing Mechanisms in Palladium-Catalyzed Alkoxycarbonylation of Styrene.

Authors :
Mehara J
Anania M
Kočovský P
Roithová J
Source :
ACS catalysis [ACS Catal] 2024 Apr 01; Vol. 14 (8), pp. 5710-5719. Date of Electronic Publication: 2024 Apr 01 (Print Publication: 2024).
Publication Year :
2024

Abstract

Palladium-catalyzed carbonylation is a versatile method for the synthesis of various aldehydes, esters, lactones, or lactams. Alkoxycarbonylation of alkenes with carbon monoxide and alcohol produces either saturated or unsaturated esters as a result of two distinct catalytic cycles. The existing literature presents an inconsistent account of the procedures favoring oxidative carbonylation products. In this study, we have monitored the intermediates featured in both catalytic cycles of the methoxycarbonylation of styrene PhCH=CH <subscript>2</subscript> as a model substrate, including all short-lived intermediates, using mass spectrometry. Comparing the reaction kinetics of the intermediates in both cycles in the same reaction mixture shows that the reaction proceeding via alkoxy intermediate [Pd <superscript>II</superscript> ]-OR, which gives rise to the unsaturated product PhCH=CHCO <subscript>2</subscript> Me, is faster. However, with an advancing reaction time, the gradually changing reaction conditions begin to favor the catalytic cycle dominated by palladium hydride [Pd <superscript>II</superscript> ]-H and alkyl intermediates, affording the saturated products PhCH <subscript>2</subscript> CH <subscript>2</subscript> CO <subscript>2</subscript> Me and PhCH(CO <subscript>2</subscript> Me)CH <subscript>3</subscript> preferentially. The role of the oxidant proved to be crucial: using p -benzoquinone results in a gradual decrease of the pH during the reaction, swaying the system from oxidative conditions toward the palladium hydride cycle. By contrast, copper(II) acetate as an oxidant guards the pH within the 5-7 range and facilitates the formation of the alkoxy palladium complex [Pd <superscript>II</superscript> ]-OR, which favors the oxidative reaction producing PhCH=CHCO <subscript>2</subscript> Me with high selectivity. Hence, it is the oxidant, rather than the catalyst, that controls the reaction outcome by a mechanistic switch. Unraveling these principles broadens the scope for developing alkoxycarbonylation reactions and their application in organic synthesis.<br />Competing Interests: The authors declare no competing financial interest.<br /> (© 2024 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2155-5435
Volume :
14
Issue :
8
Database :
MEDLINE
Journal :
ACS catalysis
Publication Type :
Academic Journal
Accession number :
38660606
Full Text :
https://doi.org/10.1021/acscatal.4c00966