Technology Process of C30H33NO2
There total 4 articles about C30H33NO2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(Z)-3'-phenylprop-2'-en-1'-yl (3R,αS,E)-3-[N-benzyl-N-(α-methylbenzyl)amino]hex-4-enoate;
With
chloro-trimethyl-silane; lithium hexamethyldisilazane;
In
tetrahydrofuran; toluene;
at -78 ℃;
for 0.25h;
In
tetrahydrofuran; toluene;
for 1h;
Overall yield = 2 g;
Reflux;
DOI:10.1039/c3cc43250e
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: trifluoroacetic acid / dichloromethane / 16 h / 20 °C
2.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 0 - 20 °C
2.2: 0 - 20 °C
3.1: chloro-trimethyl-silane; lithium hexamethyldisilazane / tetrahydrofuran; toluene / 0.25 h / -78 °C
3.2: 1 h / Reflux
With
chloro-trimethyl-silane; oxalyl dichloride; N,N-dimethyl-formamide; trifluoroacetic acid; lithium hexamethyldisilazane;
In
tetrahydrofuran; dichloromethane; toluene;
3.2: |Claisen-Ireland Rearrangement;
DOI:10.1039/c3cc43250e
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: Acidic conditions
2.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere
2.2: 2 h / -78 °C / Inert atmosphere
3.1: trifluoroacetic acid / dichloromethane / 16 h / 20 °C
4.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 0 - 20 °C
4.2: 0 - 20 °C
5.1: chloro-trimethyl-silane; lithium hexamethyldisilazane / tetrahydrofuran; toluene / 0.25 h / -78 °C
5.2: 1 h / Reflux
With
n-butyllithium; chloro-trimethyl-silane; oxalyl dichloride; N,N-dimethyl-formamide; trifluoroacetic acid; lithium hexamethyldisilazane;
In
tetrahydrofuran; hexane; dichloromethane; toluene;
5.2: |Claisen-Ireland Rearrangement;
DOI:10.1039/c3cc43250e