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Dihydropyran Formation By A Two Step Process, James Zachary Wright

Undergraduate Honors Thesis Collection

The 2, 6-disubstitued dihydropyran is produced by a two step process, involving a Suzuki Miyaura Cross Coupling reaction followed by anintramolecular ring closing Michael Addition reaction. In this project a vinyl boronic acid, 6-(2-phenylethenyl)-2-hydroxy-I,2-oxaborole, was coupled with cis-ethyl-iodo-acrylate to yield ethyI 2E, 4Z, 8E-9-phenyl-7-hydroxy-2, 4, 8-nonatrienoate, which is capable of undergoing an intramolecular Michael addition to form the dihydropyran. The geometry of the cis enolate and the conjugated double bonds of the coupled product are such that under basic conditions a Michael addition is feasible. Throughout the project, the reaction conditions for high yields of Suzuki product were determined. Dihydropyrans …