Technology Process of (E)-1-(3-(4-bromophenyl)allyl)piperidine
There total 5 articles about (E)-1-(3-(4-bromophenyl)allyl)piperidine 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: thionyl chloride / 2 h / 0 °C / Inert atmosphere; Reflux
2: diisobutylaluminium hydride / hexane; dichloromethane / 1.5 h / -78 °C / Inert atmosphere
3: phosphorus tribromide / diethyl ether / 0 °C / Inert atmosphere; Darkness
4: tetrahydrofuran / 0.17 h / 20 - 25 °C / Inert atmosphere
With
thionyl chloride; phosphorus tribromide; diisobutylaluminium hydride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja500758n
- Guidance literature:
-
Multi-step reaction with 2 steps
1: phosphorus tribromide / diethyl ether / 0 °C / Inert atmosphere; Darkness
2: tetrahydrofuran / 0.17 h / 20 - 25 °C / Inert atmosphere
With
phosphorus tribromide;
In
tetrahydrofuran; diethyl ether;
DOI:10.1021/ja500758n
- Guidance literature:
-
Multi-step reaction with 3 steps
1: diisobutylaluminium hydride / hexane; dichloromethane / 1.5 h / -78 °C / Inert atmosphere
2: phosphorus tribromide / diethyl ether / 0 °C / Inert atmosphere; Darkness
3: tetrahydrofuran / 0.17 h / 20 - 25 °C / Inert atmosphere
With
phosphorus tribromide; diisobutylaluminium hydride;
In
tetrahydrofuran; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja500758n