Alkylation of ambident 2-phenyl-1,3-indandione anion in ionic liquid medium and structure of alkylation products was written by Zicmanis, A.;Ozolina, A.;Mekss, P.;Klavins, M.. And the article was included in Latvijas Kimijas Zurnals in 2006.Synthetic Route of C17H30BrN This article mentions the following:
Alkylation of 2-phenyl-1,3-indandione anion by allyl bromide or propargyl chloride was faster in the ionic liquid 1-dodecylpyridinium bromide than in a phase-transfer system. Only C-alkylation products were formed, and the cation used had no appreciable effect. In the experiment, the researchers used many compounds, for example, 1-Dodecylpyridin-1-ium bromide (cas: 104-73-4Synthetic Route of C17H30BrN).
1-Dodecylpyridin-1-ium bromide (cas: 104-73-4) belongs to pyridine derivatives. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Synthetic Route of C17H30BrN