A Tribute to Ullmann’s Work: Expanding Copper Coil Reactor Applications toward the Hydroxylation of Aryl Bromides

dc.contributor
Universitat Ramon Llull. IQS
dc.contributor.author
Molins Colomer, Maite
dc.contributor.author
Fernandez Garcia, Javier
dc.contributor.author
Berzosa, Xavier
dc.date.accessioned
2025-06-07T11:13:27Z
dc.date.available
2025-06-07T11:13:27Z
dc.date.issued
2024-12-08
dc.identifier.issn
1520-586X
dc.identifier.uri
http://hdl.handle.net/20.500.14342/5298
dc.description.abstract
Copper coil flow reactors represent an economic, abundant, and durable platform for conducting copper-catalyzed reactions. These have been used in the past for Ullmann-type reactions starting from aryl iodides. However, no procedures have been described for the activation of less reactive aryl bromides. In this work, we successfully developed a method for the hydroxylation of aryl bromides promoted by a copper coil reactor. Notably, the presence of both a diamine ligand and DMF is key for the reaction to proceed. An inorganic base such as Na2CO3 also improved the reaction yield by minimizing the formation of side products. The setup has been applied to a range of disubstituted aryl bromides in moderate to good yields and was tested under 24 h of continuous operation, showing stable yields, thus proving the robustness of the catalysis. Finally, the lifetime of a copper reactor operating under the described conditions has been calculated for the first time, proving that this technology is safe to operate at an industrial scale.
dc.format.extent
8 p.
dc.language.iso
eng
dc.publisher
American Chemical Society
dc.relation.ispartof
Organic Process Research & Development. 2024;28(12):4477-4484
dc.rights
© L'autor/a
dc.rights
Attribution 4.0 International
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
aryl halides
dc.subject
C−O bond formation
dc.subject
copper
dc.subject
flow chemistry
dc.subject
hydroxylation
dc.subject
phenols
dc.title
A Tribute to Ullmann’s Work: Expanding Copper Coil Reactor Applications toward the Hydroxylation of Aryl Bromides
dc.type
info:eu-repo/semantics/article
dc.subject.udc
544
dc.description.version
info:eu-repo/semantics/publishedVersion
dc.embargo.terms
cap
dc.relation.projectID
info:eu-repo/grantAgreement/SUR del DEC/SGR/2021 SGR 00520
dc.relation.projectID
info:eu-repo/grantAgreement/SUR del DEC/SGR/2021 SGR 00321
dc.relation.projectID
info:eu-repo/grantAgreement/MICIU/FPU/21/05233
dc.identifier.doi
https://doi.org/10.1021/acs.oprd.4c00402
dc.rights.accessLevel
info:eu-repo/semantics/openAccess


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