Technology Process of 3-(7-chloroheptyloxy)-6-(4-(11-(1,1,1,3,3,5,5-heptamethyltrisiloxanyl)undecyloxy)phenyl)pyridazine
There total 5 articles about 3-(7-chloroheptyloxy)-6-(4-(11-(1,1,1,3,3,5,5-heptamethyltrisiloxanyl)undecyloxy)phenyl)pyridazine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 20 ℃;
Inert atmosphere;
DOI:10.1039/c1cc10344j
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium hydride / tetrahydrofuran / 1 h
1.2: 20 °C
2.1: hydrogenchloride / water; isopropyl alcohol / 5 h / 50 °C
3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere
With
hydrogenchloride; di-isopropyl azodicarboxylate; sodium hydride; triphenylphosphine;
In
tetrahydrofuran; water; isopropyl alcohol;
3.1: Mitsunobu reaction;
DOI:10.1039/c1cc10344j
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: tris-(dibenzylideneacetone)dipalladium(0); potassium phosphate; tricyclohexylphosphine / 1,4-dioxane; water / 18 h / 100 °C / Inert atmosphere
2.1: sodium hydride / tetrahydrofuran / 1 h
2.2: 20 °C
3.1: hydrogenchloride / water; isopropyl alcohol / 5 h / 50 °C
4.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere
With
hydrogenchloride; potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); di-isopropyl azodicarboxylate; sodium hydride; triphenylphosphine; tricyclohexylphosphine;
In
tetrahydrofuran; 1,4-dioxane; water; isopropyl alcohol;
4.1: Mitsunobu reaction;
DOI:10.1039/c1cc10344j