Technology Process of 2-Piperidinone, 1-methyl-3-phenyl-
There total 5 articles about 2-Piperidinone, 1-methyl-3-phenyl- 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:
-
With
palladium 10% on activated carbon; hydrogen;
In
ethanol;
at 20 ℃;
for 24h;
under 760.051 Torr;
DOI:10.1021/jo502362k
- Guidance literature:
-
With
dicobalt octacarbonyl;
In
benzene;
at 200 - 220 ℃;
for 72h;
under 41040 Torr;
Product distribution;
Mechanism;
other substituted nitrogen heterocyclics; also Co2(CO)8/Ru3(CO)12 catalyzed rearrangement reactions;
DOI:10.1021/ja00044a010
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: potassium tert-butylate / 1,4-dioxane / 2 h / 100 °C / Schlenk technique; Inert atmosphere
1.2: 16 h / 80 °C / Schlenk technique; Inert atmosphere
2.1: bis-triphenylphosphine-palladium(II) chloride; sodium carbonate / toluene; ethanol; water / 16 h / 80 °C / Schlenk technique; Inert atmosphere
3.1: potassium tert-butylate; [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); 1,3-bis-(1(R)-phenyl-ethyl)-4,5-dihydro-3H-imidazol-1-ium tetrafluoroborate; hydrogen / hexane; tert-Amyl alcohol / 24 h / 25 °C / 90009 Torr / Glovebox; Schlenk technique; Autoclave
With
bis-triphenylphosphine-palladium(II) chloride; [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); 1,3-bis-(1(R)-phenyl-ethyl)-4,5-dihydro-3H-imidazol-1-ium tetrafluoroborate; potassium tert-butylate; hydrogen; sodium carbonate;
In
1,4-dioxane; tert-Amyl alcohol; ethanol; hexane; water; toluene;
DOI:10.1055/s-0034-1378703