Technology Process of N-benzyl-N-(6,7-dimethoxy-4-methyl-3,4-dihydronaphthalen-2-yl)benzamide
There total 6 articles about N-benzyl-N-(6,7-dimethoxy-4-methyl-3,4-dihydronaphthalen-2-yl)benzamide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: potassium tert-butylate / diethyl ether / 0.75 h / 20 °C / Inert atmosphere
1.2: 125 °C / Inert atmosphere
2.1: toluene / Reflux; Inert atmosphere
3.1: triethylamine / dichloromethane / 20 °C / Inert atmosphere; Cooling with ice
With
potassium tert-butylate; triethylamine;
In
diethyl ether; dichloromethane; toluene;
1.1: Dieckmann condensation;
DOI:10.1021/jm200334c
- Guidance literature:
-
Multi-step reaction with 2 steps
1: toluene / Reflux; Inert atmosphere
2: triethylamine / dichloromethane / 20 °C / Inert atmosphere; Cooling with ice
With
triethylamine;
In
dichloromethane; toluene;
DOI:10.1021/jm200334c
- Guidance literature:
-
Multi-step reaction with 7 steps
1.1: Iodine monochloride; acetic acid / dichloromethane / Inert atmosphere
2.1: Amberlyst / Inert atmosphere
3.1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / acetonitrile / 96 h / Inert atmosphere; Reflux
4.1: hydrogen / ethanol / 3102.97 Torr
5.1: potassium tert-butylate / diethyl ether / 0.75 h / 20 °C / Inert atmosphere
5.2: 125 °C / Inert atmosphere
6.1: toluene / Reflux; Inert atmosphere
7.1: triethylamine / dichloromethane / 20 °C / Inert atmosphere; Cooling with ice
With
bis-triphenylphosphine-palladium(II) chloride; potassium tert-butylate; hydrogen; Iodine monochloride; acetic acid; triethylamine;
In
diethyl ether; ethanol; dichloromethane; toluene; acetonitrile;
3.1: Heck reaction / 5.1: Dieckmann condensation;
DOI:10.1021/jm200334c