In 2004,Anders, Joachim T.; Langer, Peter published 《Domino cyclization/electrocyclization/elimination reactions of arylacetonitriles with N,N’-bis(1-naphthyl)oxaldiimidoyl dichlorides: Efficient synthesis of fluorescent 15H-benzo[h]benzo[6,7]indolo[3,2-b]quinolines》.European Journal of Organic Chemistry published the findings.Synthetic Route of C8H6BrN The information in the text is summarized as follows:
15H-Benzo[h]benzo[6,7]indolo[3,2-b]quinolines, e.g., I, were prepared by domino cyclization/electrocyclization/elimination reactions of nitriles with N,N’-bis(1-naphthyl)oxaldiimidoyl dichlorides. The products can be regarded as hexacyclic δ-carbolines and were fluorescent dyes.2-(3-Bromophenyl)acetonitrile(cas: 31938-07-5Synthetic Route of C8H6BrN) was used in this study.
2-(3-Bromophenyl)acetonitrile(cas: 31938-07-5) has been used in the synthesis of 2-(1-cyano-1-(3-bromophenyl))methylidene-3-phenylthiazolidine-4,5-dione or a series of aminoethylbiphenyls, novel 5-HT7 receptor ligands.Synthetic Route of C8H6BrN
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts