Synthesis 2015; 47(08): 1091-1100
DOI: 10.1055/s-0034-1379992
paper
© Georg Thieme Verlag Stuttgart · New York

Proximity- and Chelation-Induced SNAr 1,4-Aromatic ortho-Substitution of ortho-Methoxyphenyl 2-Alkyl Ketones

Gwendal Grelier
Department of Chemistry, Université de Montréal, Station Centre-Ville, C. P. 6128, Montréal, Quebec H3C 3J7, Canada   Email: stephen.hanessian@umontreal.ca
,
Etienne Chénard
Department of Chemistry, Université de Montréal, Station Centre-Ville, C. P. 6128, Montréal, Quebec H3C 3J7, Canada   Email: stephen.hanessian@umontreal.ca
,
Martin Büschleb
Department of Chemistry, Université de Montréal, Station Centre-Ville, C. P. 6128, Montréal, Quebec H3C 3J7, Canada   Email: stephen.hanessian@umontreal.ca
,
Stephen Hanessian*
Department of Chemistry, Université de Montréal, Station Centre-Ville, C. P. 6128, Montréal, Quebec H3C 3J7, Canada   Email: stephen.hanessian@umontreal.ca
› Author Affiliations
Further Information

Publication History

Received: 20 November 2014

Accepted after revision: 22 December 2014

Publication Date:
12 February 2015 (online)


Abstract

The direct displacement of an o-methoxy group in o-methoxyaryl ketones with aryl, alkyl, and alkenyl Grignard reagents to provide a series of o-substituted ketones is described. Application of this reaction to the synthesis of a C-methyl analogue of a cyclooxygenase inhibitor is shown. The scope and limitations are discussed.

Supporting Information