Technology Process of C15H17NO
There total 8 articles about C15H17NO 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: toluene / 2 h / 25 °C / Reflux
2.1: 1,1'-carbonyldiimidazole / chloroform / 14 h / Inert atmosphere; Reflux
3.1: diisobutylaluminium hydride / dichloromethane; hexane / 0.5 h / -78 °C / Inert atmosphere
3.2: 2 h / 0 °C / Inert atmosphere
4.1: acetone / 50 °C
With
diisobutylaluminium hydride; 1,1'-carbonyldiimidazole;
In
hexane; dichloromethane; chloroform; acetone; toluene;
DOI:10.1039/c2cc37123e
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: diisobutylaluminium hydride / dichloromethane; hexane / 0.5 h / -78 °C / Inert atmosphere
1.2: 2 h / 0 °C / Inert atmosphere
2.1: acetone / 50 °C
With
diisobutylaluminium hydride;
In
hexane; dichloromethane; acetone;
DOI:10.1039/c2cc37123e
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: N,N-dimethyl-formamide / 5 h / 25 °C
2.1: boron trifluoride diethyl etherate / o-xylene; diethyl ether / 2 h / -10 - 165 °C / Microwave irradiation
3.1: toluene / 2 h / 25 °C / Reflux
4.1: 1,1'-carbonyldiimidazole / chloroform / 14 h / Inert atmosphere; Reflux
5.1: diisobutylaluminium hydride / dichloromethane; hexane / 0.5 h / -78 °C / Inert atmosphere
5.2: 2 h / 0 °C / Inert atmosphere
6.1: acetone / 50 °C
With
boron trifluoride diethyl etherate; diisobutylaluminium hydride; 1,1'-carbonyldiimidazole;
In
diethyl ether; hexane; dichloromethane; chloroform; o-xylene; N,N-dimethyl-formamide; acetone; toluene;
2.1: |Claisen Rearrangement;
DOI:10.1039/c2cc37123e
