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N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide

Base Information
  • Chemical Name:N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide
  • CAS No.:1453905-15-1
  • Molecular Formula:C48H42Br2N2O4
  • Molecular Weight:870.68
  • Hs Code.:
N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide

Synonyms:N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide

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Chemical Property of N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide
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Technology Process of N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide

There total 3 articles about N,N’-bis(4-bromo-2,6-diisopropyl)-4,4’-binaphthyl-1,1’,8,8’-teracarboxylic bisimide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 2 steps
1: zinc; nickel dibromide; triphenylphosphine / N,N-dimethyl acetamide / 7 h / 85 °C / Inert atmosphere
2: zinc(II) chloride hexahydrate; 1H-imidazole / 24 h / 140 °C / Inert atmosphere
With 1H-imidazole; zinc(II) chloride hexahydrate; triphenylphosphine; nickel dibromide; zinc; In N,N-dimethyl acetamide;
DOI:10.1021/ol401946g
Guidance literature:
Multi-step reaction with 3 steps
1: 1,8-diazabicyclo[5.4.0]undec-7-ene / methanol / 3 h / 60 °C
2: nickel dibromide; triphenylphosphine; zinc / N,N-dimethyl acetamide / 85 °C
3: 1H-imidazole; zinc(II) chloride / 140 °C
With 1H-imidazole; 1,8-diazabicyclo[5.4.0]undec-7-ene; triphenylphosphine; zinc(II) chloride; nickel dibromide; zinc; In methanol; N,N-dimethyl acetamide;
DOI:10.1021/acs.chemmater.5b04602
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