Abstract:
The bromination reaction of benz[f]indan-1-one was investigated by NBS. molecular bromine and fotobromination. Benz[f]indart-1-one was synthesized by treatment of alpha,alpha,alpha',alpha'-tetrabromo-o-xylene with cyclopenten-1-one. Bromination of benz[f]indan-1-one with bromine (1.2 equiv) at low temperature afforded the alpha-monobromobenz[f]indanone in addition to alpha,alpha'-dibromobenz[f]indanone. The quantitative yield of alpha,alpha'-dibromobenz[f]indanone was synthesized by treatment of benz[f]indan-1-one with 2.1 equv. bromine at room temperature for 25 min. The electrophonic bromination of alpha,alpha'-dibromobenz[f]indanone with N-bromosuccinimide (NBS) regioselectively proceeded at C-8 side and afforded the corresponding 2,2,8-Tribromobenz[f]indanone which also could be obtained from the treatment of benz[f]indan-1-one with NBS and SiO2. Dibromobenz[f]indenone was generated by the treatment of benz[f]indan-1-one with bromine in photochemical reaction apparatus irradiated by 150 watt projection lamp. Dibromobenz[f]indenone was also synthesized by the treatment of alpha,alpha'-dibromobenz[f]indanone with NBS in photochemical reaction apparatus irradiated by 150 watt projection lamp. 2.8-Dibromobenz[f]indanone was synthesized by the reaction of alpha-monobromobenz[f]indanone with NBS.
