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C25H12BrN

Base Information Edit
C<sub>25</sub>H<sub>12</sub>BrN

Synonyms:C25H12BrN

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C25H12BrN Edit
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Technology Process of C25H12BrN

There total 1 articles about C25H12BrN 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:
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); In N,N-dimethyl-formamide; at 80 ℃;
DOI:10.1016/j.tetlet.2011.06.089
Guidance literature:
C25H12BrN; trimethylsilylacetylene; With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine; In toluene; at 90 ℃;
With potassium carbonate; In tetrahydrofuran; methanol; at 20 ℃; for 2h;
DOI:10.1016/j.tetlet.2011.06.089
Guidance literature:
Multi-step reaction with 3 steps
1.1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / toluene / 90 °C
1.2: 2 h / 20 °C
2.1: copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine / N,N-dimethyl-formamide / 2 h / 80 °C
3.1: ammonium hydroxide / methanol / 60 °C
With ammonium hydroxide; copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine; In methanol; N,N-dimethyl-formamide; toluene; 1.1: Sonogashira cross-coupling / 2.1: Sonogashira cross-coupling;
DOI:10.1016/j.tetlet.2011.06.089
upstream raw materials:

1,6-dibromopyrene

4-cyanophenylacetylene

Downstream raw materials:

C38H25N5O3

C38H25N5O4

C41H30N6O3

C27H13N

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