115679-97-5

Upstream product

• 4356-69-8 1,1-bis-(4-methoxyphenyl)ethylene 
• 90-99-3 diphenylchloromethane 
• 776-74-9 Bromodiphenylmethane 
• 2657-24-1 1-(4-methoxyphenyl)-3,3-diphenylpropan-1-one 
• 13139-86-1 4-methoxyphenyl magnesium bromide 

Downstream Products

• 947-91-1 Diphenylacetaldehyde 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 129919-67-1 1,1-Bis(4-methoxyphenyl)-trans-2,3-diphenylcyclopropane 
• 129919-68-2 3,3-Bis(4-methoxyphenyl)-cis-4,5-diphenyl-1,2-dioxolane 
• 129919-68-2 3,3-Bis(4-methoxyphenyl)-trans-4,5-diphenyl-1,2-dioxolane 
• 124141-45-3 1,1-di(4-methoxyphenyl)-3,3-diphenyl-1,2-propadiene 

Relevant academic research and scientific papers

Electron-Transfer-Induced Photorearrangements and Photooxygenations of 1,1,2,3-Tetraarylcyclopropanes

1,1-Diaryl-trans-2,3-diphenylcyclopropanes 3a-e and trans-2,3-diaryl-1,1-diphenylcyclopropanes 3f-i were prepared by di-?-methane rearrangement of 1,1-diaryl-3,3-diphenylpropenes 2a-e and 3,3-diaryl-1,1-diphenylpropenes 2f-i, respectively.In nonpolar and in polar solvents, tetraarylcyclopropanes 3a-i are inert toward singlet oxygen.In the presence of 9,10-dicyanoanthracene (DCA), irradiation of cyclopropanes 3a-e in O2-saturated acetonitrile (MeCN) solutions yield oxygenation products: benzophenone and benzaldehyde as main products from 3a, 1,2-dioxolanes 4b-e from3b-e.Cyclopropanes 3f-i, however, rearrange to 3,3-diaryl-1,1-diphenylpropenes 2f-i under these conditions.When irridiated in the presence of DCA or 1,8-dihydroxyanthraquinone (1,8-AQ) in deoxygenated MeCN solutions, Cyclopropanes 3a-e remain unchanged, whereas cyclopropanes 3f-i rearrange to propenes 2f-i.By using biphenyl and lithium perchlorate as additives in DCA-sensitized reactions, photooxygenations of 3a-e as well as photorearrangements of 3f-i are shown to proceed as electron-transfer-induced reactions via 1,3-radical cations formed by ring opening, occurring in all cases exclusively between carbon atoms C-1 and C-2 of these cyclopropanes.Small amounts of benzoquinone quench the DCA-sensitized oxygenation of cyclopropanes 3a-e completely, and 1,8-AQ is incapable of sensitizing the oxygenations of these cyclopropanes, indicating that electron-transfer-induced oxygenations of 1,1,2,3-tetraarylcyclopropanes need superoxide radical anion, O2.-, as the oxygenating species.A mechanism is proposed according to which the cationic sites of the 1,3-radical cation intermediates determine whether the respective radical cation rearr anges rapidly by 1,2-aryl migration to the corresponding 1,1,3,3-tetraarylpropene or is long lived enough to undergo a bimolecular reaction with O2.- to yield the corresponding 1,2-dioxolane.