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C25H32BrNO4

Base Information Edit
C<sub>25</sub>H<sub>32</sub>BrNO<sub>4</sub>

Synonyms:C25H32BrNO4

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C25H32BrNO4 Edit
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Technology Process of C25H32BrNO4

There total 4 articles about C25H32BrNO4 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 dmap; triethylamine; In dichloromethane; at 20 ℃; for 12h; Cooling with ice;
DOI:10.1016/j.bmcl.2012.05.124
Guidance literature:
Multi-step reaction with 3 steps
1: hydrogenchloride / water; toluene / Reflux
2: sodium cyanoborohydride / ethanol / 20 °C / Cooling with ice
3: dmap; triethylamine / dichloromethane / 12 h / 20 °C / Cooling with ice
With hydrogenchloride; dmap; sodium cyanoborohydride; triethylamine; In ethanol; dichloromethane; water; toluene;
DOI:10.1016/j.bmcl.2012.05.124
Guidance literature:
Multi-step reaction with 4 steps
1: potassium carbonate / N,N-dimethyl-formamide / 24 h / Inert atmosphere; Reflux
2: hydrogenchloride / water; toluene / Reflux
3: sodium cyanoborohydride / ethanol / 20 °C / Cooling with ice
4: dmap; triethylamine / dichloromethane / 12 h / 20 °C / Cooling with ice
With hydrogenchloride; dmap; sodium cyanoborohydride; potassium carbonate; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; 1: Williamson etherification;
DOI:10.1016/j.bmcl.2012.05.124
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