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  • A general method for the synthesis of 3,5-diarylcyclopentenones via friedel-crafts acylation of vinyl chlorides.

A general method for the synthesis of 3,5-diarylcyclopentenones via friedel-crafts acylation of vinyl chlorides.

The Journal of organic chemistry (2009-06-03)
Yingju Xu, Mark McLaughlin, Cheng-yi Chen, Robert A Reamer, Peter G Dormer, Ian W Davies
ABSTRACT

A general approach for the synthesis of 3,5-diarylcyclopentenones was developed. Key aspects of this approach are the intramolecular Friedel-Crafts-type cyclization of vinyl chlorides and subsequent Pd-catalyzed cross-coupling reactions. The requisite vinyl chloride-bearing arylacetic acid precursors are readily available by straightforward alkylation of arylacetic acid esters and undergo cyclization to yield 3-chloro-5-aryl-2-cyclopentenones when treated with AlCl(3). The vinylogous acid chloride functionality present in these immediate products allows for further elaboration via Pd-catalyzed cross-coupling chemistry, leading to a diverse array of products.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
1-Penten-3-one, contains 0.1% BHT as stabilizer, 97%