Technology Process of N-(3-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-2,2-dimethylpropyl)benzamide
There total 4 articles about N-(3-(1,4-dioxo-1,4-dihydronaphthalen-2-yl)-2,2-dimethylpropyl)benzamide which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: boron tribromide / dichloromethane / 0.2 h / -78 °C
1.2: 0 °C
2.1: potassium nitrososulfonate / methanol; water; N,N-dimethyl-formamide / 10 h / 20 °C
With
potassium nitrososulfonate; boron tribromide;
In
methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.020
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran / 3.08 h / 0 - 20 °C
1.2: 20 °C
2.1: 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride / methanol / 1 h / 20 °C
3.1: boron tribromide / dichloromethane / 0.2 h / -78 °C
3.2: 0 °C
4.1: potassium nitrososulfonate / methanol; water; N,N-dimethyl-formamide / 10 h / 20 °C
With
lithium aluminium tetrahydride; potassium nitrososulfonate; boron tribromide; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.020
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: n-butyllithium; diisopropylamine / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere
1.2: 2 h / -78 °C / Inert atmosphere
2.1: lithium aluminium tetrahydride / tetrahydrofuran / 3.08 h / 0 - 20 °C
2.2: 20 °C
3.1: 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride / methanol / 1 h / 20 °C
4.1: boron tribromide / dichloromethane / 0.2 h / -78 °C
4.2: 0 °C
5.1: potassium nitrososulfonate / methanol; water; N,N-dimethyl-formamide / 10 h / 20 °C
With
lithium aluminium tetrahydride; n-butyllithium; potassium nitrososulfonate; boron tribromide; diisopropylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2012.01.020