Yılmaz, MakbuleTutar, AhmetErenler, Ramazan2020-04-302020-04-3020131747-5198https://doi.org/10.3184/174751913X13636300018867https://hdl.handle.net/20.500.12684/4721Erenler, Ramazan/0000-0002-0505-3190; Tutar, Ahmet/0000-0001-5524-8001WOS: 000318899400013The bromination reactions of 5-aminoindane, 5-acetamidoindane, and 5-acetamidoindan-1-one were investigated using NBS, molecular bromine and photobromination, and the optimum reaction conditions were presented. The reaction of 5-aminoindane with glacial acetic acid at reflux temperature resulted in the formation of 5-acetamidoindane in high yield. 5-Acetamidoindan-1-one was generated by the reaction of 5-acetamidoindane with CrO3 in acetic acid. Selective bromination at C-6 position of 5-acetamidoindane was achieved by treatment of title compound with bromine in acetic acid and thus afforded 5-acetamido-6-bromoindane. Further bromination reactions of bromoindanones were achieved in various reaction conditions.en10.3184/174751913X13636300018867info:eu-repo/semantics/closedAccessbromination reactionsbromoaminoindanebromoaminoindanoneArticle4232235WOS:000318899400013Q3Q4