Technology Process of (4S)-4-benzyl-2-(furan-2-ylvinyl)-2-oxazoline
There total 4 articles about (4S)-4-benzyl-2-(furan-2-ylvinyl)-2-oxazoline which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
thionyl chloride; potassium carbonate; sodium bromide;
In
acetonitrile;
for 4h;
Reflux;
DOI:10.1016/j.tetasy.2013.12.003
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: dicyclohexyl-carbodiimide; dmap / dichloromethane / 12 h / 20 °C / Inert atmosphere
2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere
2.2: 4 h / 20 °C / Inert atmosphere
3.1: thionyl chloride; potassium carbonate; sodium bromide / acetonitrile / 4 h / Reflux
With
dmap; thionyl chloride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; dicyclohexyl-carbodiimide; sodium bromide;
In
tetrahydrofuran; dichloromethane; acetonitrile;
2.1: |Horner-Wadsworth-Emmons Olefination / 2.2: |Horner-Wadsworth-Emmons Olefination;
DOI:10.1016/j.tetasy.2013.12.003
- Guidance literature:
-
Multi-step reaction with 2 steps
1: (bis-(2-methoxyethyl)amino)sulfur trufluoride; potassium carbonate / dichloromethane / -20 °C
2: N,N-dimethyl-formamide / 2 h / Reflux
With
potassium carbonate; (bis-(2-methoxyethyl)amino)sulfur trufluoride;
In
dichloromethane; N,N-dimethyl-formamide;
2: |Horner-Wadsworth-Emmons Olefination;
DOI:10.1016/j.tetasy.2013.12.003