Technology Process of 2,2-dimethyl-4-oxo-3,8,11,14,17,20,23-heptaoxa-5-azapentacosan-25-yl 4-methylbenzenesulfonate
There total 8 articles about 2,2-dimethyl-4-oxo-3,8,11,14,17,20,23-heptaoxa-5-azapentacosan-25-yl 4-methylbenzenesulfonate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
t-butyl 20-hydroxy-3,6,9,12,15,18-hexaoxaicosylcarbamate;
With
triethylamine;
In
dichloromethane;
at 0 ℃;
for 0.0833333h;
p-toluenesulfonyl chloride;
In
dichloromethane;
at 0 - 20 ℃;
for 24h;
DOI:10.1002/ejoc.201001666
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: ethanol / 0 - 20 °C
2.1: dmap; triethylamine / dichloromethane / 20 °C / Inert atmosphere
3.1: sodium hydroxide / water; toluene / 1 h / 100 °C
3.2: 20 - 100 °C
4.1: triethylamine / dichloromethane / 0.08 h / 0 °C
4.2: 24 h / 0 - 20 °C
With
dmap; triethylamine; sodium hydroxide;
In
ethanol; dichloromethane; water; toluene;
DOI:10.1002/ejoc.201001666
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C / 760.05 Torr
2.1: ethanol / 0 - 20 °C
3.1: dmap; triethylamine / dichloromethane / 20 °C / Inert atmosphere
4.1: sodium hydroxide / water; toluene / 1 h / 100 °C
4.2: 20 - 100 °C
5.1: triethylamine / dichloromethane / 0.08 h / 0 °C
5.2: 24 h / 0 - 20 °C
With
dmap; palladium 10% on activated carbon; hydrogen; triethylamine; sodium hydroxide;
In
ethanol; dichloromethane; water; toluene;
DOI:10.1002/ejoc.201001666