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<1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril

Base Information
  • Chemical Name:<1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril
  • CAS No.:158611-45-1
  • Molecular Formula:C20H15N3O2
  • Molecular Weight:329.358
  • Hs Code.:
<1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril

Synonyms:<1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril

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Chemical Property of <1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril
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Technology Process of <1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril

There total 4 articles about <1-Ethyl-6-hydroxy-2-(4-hydroxyphenyl)-indol-3-yl>-methylidenmalonsaeuredinitril 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 4 steps
1: 1.) 80percent NaH / 1.) DMF, 0 deg C, 1 h, 2.) DMF, 0 deg C, 30 min; r.t., 2 h
2: 82 percent / POCl3 / 1.5 h / 35 °C
3: BBr3 / CH2Cl2 / 2 h / Ambient temperature
4: 79 percent / β-alanin / ethanol / 24 h / Ambient temperature
With boron tribromide; sodium hydride; 3-amino propanoic acid; trichlorophosphate; In ethanol; dichloromethane;
DOI:10.1002/ardp.19943270804
Guidance literature:
Multi-step reaction with 3 steps
1: 82 percent / POCl3 / 1.5 h / 35 °C
2: BBr3 / CH2Cl2 / 2 h / Ambient temperature
3: 79 percent / β-alanin / ethanol / 24 h / Ambient temperature
With boron tribromide; 3-amino propanoic acid; trichlorophosphate; In ethanol; dichloromethane;
DOI:10.1002/ardp.19943270804
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