2014
DOI: 10.3390/molecules19055876
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Cobalt-Catalyzed Methoxycarbonylation of Substituted Dichlorobenzenes as an Example of a Facile Radical Anion Nucleophilic Substitution in Chloroarenes

Abstract: A thorough mechanistic study on cobalt-catalysed direct methoxycarbonylation reactions of chlorobenzenes in the presence of methyl oxirane on a wide range of substrates, including poly-and monochloro derivatives with multiple substituents, is reported. The results demonstrate that the reaction is potentially useful as it proceeds under very mild conditions (t = 62 °C, P CO = 1 bar) and converts aryl chlorides to far more valuable products (especially ortho-substituted benzoic acids and esters) in high yields. … Show more

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Cited by 10 publications
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“…A similar process of cyclization with participation of two carbonyl groups in the ortho-position in benzene ring is known for chemical reaction in solution. It explains, for instance, the formation of 6-chloro-3-methoxyphthalide from 2-acetyl-5-chlorobenzoic acid [21]:…”
Section: Features Of Gc Separation Of Monoalkyl Phthalatesmentioning
confidence: 99%
“…A similar process of cyclization with participation of two carbonyl groups in the ortho-position in benzene ring is known for chemical reaction in solution. It explains, for instance, the formation of 6-chloro-3-methoxyphthalide from 2-acetyl-5-chlorobenzoic acid [21]:…”
Section: Features Of Gc Separation Of Monoalkyl Phthalatesmentioning
confidence: 99%