Technology Process of (2S,3R,14E)-2-aminooctadecen-3-ol
There total 10 articles about (2S,3R,14E)-2-aminooctadecen-3-ol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogenchloride;
In
1,4-dioxane;
at 0 ℃;
for 3.16667h;
DOI:10.1194/jlr.M067033
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: toluene-4-sulfonic acid / tetrahydrofuran; dichloromethane / 12 h / 0 - 20 °C
2.1: carbon tetrabromide; triphenylphosphine / dichloromethane / 4 h / 0 - 20 °C
3.1: tert.-butyl lithium / toluene / 1 h / -78 °C
3.2: 7 h / -78 - 20 °C
4.1: ethylenediamine; hydrogen / N,N-dimethyl-formamide; ethyl acetate / 6 h / 0 °C
5.1: pyridinium p-toluenesulfonate / ethanol / 2 h / 62 °C
6.1: carbon tetrabromide; triphenylphosphine / dichloromethane / 4 h / 0 - 20 °C
7.1: magnesium / diethyl ether / 2 h / Reflux
7.2: 2 h / Reflux
8.1: lithium tri-t-butoxyaluminum hydride / ethanol / 1 h / -78 °C
9.1: hydrogenchloride / 1,4-dioxane / 3.17 h / 0 °C
With
hydrogenchloride; carbon tetrabromide; hydrogen; tert.-butyl lithium; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; magnesium; lithium tri-t-butoxyaluminum hydride; ethylenediamine; triphenylphosphine;
In
tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; toluene;
2.1: |Appel Halogenation / 6.1: |Appel Halogenation;
DOI:10.1194/jlr.M067033