| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5216986 | Tetrahedron | 2014 | 5 Pages |
Abstract
The system formed by combining in situ Pd(OAc)2 with (2-pyridyl)diphenylphosphine (PyPPh2) and CH3SO3H catalyzes efficiently the carbonylation of terminal alkynes (phenylacetylene or 1-hexyne) with alcohols having perfluorinated segments of the type CF3(CF2)m(CH2)n-OH (m=1 or 3, n=1, 2 or 3) or with pentafluorophenol. Good carbonylation rates accompanied by high regioselectivity towards acrylate ester formation are obtained under mild reaction conditions (T=60-80 °C, P(CO)=30 atm). The influence of the CO pressure, the catalyst composition, the temperature and the number (n) of protonated methylene groups on the catalysis has been studied.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Alberto Scrivanti, Matteo Bertoldini, Manuela Aversa, Valentina Beghetto, Aurora Zancanaro, Stefano Paganelli, Ugo Matteoli,